rizatriptan has been researched along with Acute Disease in 36 studies
rizatriptan: structure given in first source; RN given refers to benzoate
Acute Disease: Disease having a short and relatively severe course.
Excerpt | Relevance | Reference |
---|---|---|
"Rizatriptan 10-mg ODT was superior to placebo at all pain end points for treatment of acute migraine in patients using topiramate for migraine prophylaxis." | 2.77 | Rizatriptan for treatment of acute migraine in patients taking topiramate for migraine prophylaxis. ( Cady, RK; Connor, KM; Ge, Y; Ho, TW; Hustad, CM; MacGregor, A; Schaefer, E; Seeburger, JL; Strickler, N; Valade, D; Winner, P; Zhang, Y, 2012) |
"Frovatriptan was as effective as rizatriptan in the immediate treatment of menstrually related migraine attacks while showing a favorable sustained effect with a lower rate of migraine recurrence." | 2.76 | Efficacy of frovatriptan in the acute treatment of menstrually related migraine: analysis of a double-blind, randomized, cross-over, multicenter, Italian, comparative study versus rizatriptan. ( Ferrari, MD; Lisotto, C; Omboni, S; Pinessi, L; Savi, L; Zanchin, G; Zava, D, 2011) |
"Eligible patients with migraine according to International Headache Society criteria treated a single migraine attack of moderate or severe intensity within 4 h from pain onset." | 2.73 | Efficacy and tolerability of coadministration of rizatriptan and acetaminophen vs rizatriptan or acetaminophen alone for acute migraine treatment. ( Diamond, M; Diamond, S; Freitag, F; Janssen, I; Rodgers, A; Skobieranda, F, 2008) |
"Adult women with ICHD-II menstrual migraine were assigned to either rizatriptan 10-mg tablet or placebo in a 2 : 1 ratio." | 2.73 | Rizatriptan for the acute treatment of ICHD-II proposed menstrual migraine: two prospective, randomized, placebo-controlled, double-blind studies. ( Hustad, CM; Loder, E; Mannix, LK; Mueller, L; Nett, R; Ramsey, KE; Rodgers, A; Skobieranda, F, 2007) |
"One hundred and fifty-five migraine patients were randomised to rizatriptan 10 mg (53), ibuprofen 400 mg (52) and placebo (50)." | 2.73 | Rizatriptan vs. ibuprofen in migraine: a randomised placebo-controlled trial. ( Kalita, J; Misra, UK; Yadav, RK, 2007) |
"TAME (Treat A Migraine Early)1 was conducted at 46 centers in the United States; TAME2, at 48 centers in the United States." | 2.72 | Efficacy of Rizatriptan 10 mg administered early in a migraine attack. ( Cady, R; Hustad, CM; Martin, V; Mauskop, A; Ramsey, KE; Rodgers, A; Skobieranda, F, 2006) |
"Gastroparesis frequently happens during migraine attacks, postponing the onset of action of orally administered drugs." | 2.72 | Rizatriptan vs. rizatriptan plus trimebutine for the acute treatment of migraine: a double-blind, randomized, cross-over, placebo-controlled study. ( Bigal, ME; Filho, PF; Krymchantowski, AV, 2006) |
"Adult migraineurs treated two migraine attacks with either rizatriptan 10-mg standard tablets or rizatriptan 10-mg orally disintegrating tablets in a crossover manner." | 2.71 | Real-world experiences in migraine therapy with rizatriptan. ( Cutrer, FM; Dayno, J; Goldstein, J; Hu, XH; Jamieson, D, 2003) |
"Patients with IHS migraine were randomized to one out of 3 groups, where they had to treat 6 consecutive moderate or severe attacks in counterbalanced order." | 2.71 | Rizatriptan versus rizatriptan plus rofecoxib versus rizatriptan plus tolfenamic acid in the acute treatment of migraine. ( Bigal, ME; Krymchantowski, AV, 2004) |
"Rizatriptan 5 mg was well tolerated in both the studies, with an adverse event profile not significantly different from that of placebo or standard care." | 2.71 | Rizatriptan 5 mg for the acute treatment of migraine in adolescents: results from a double-blind, single-attack study and two open-label, multiple-attack studies. ( Cady, R; Klipfel, M; Lewis, D; McCarroll, K; Nett, R; Peng, Y; Strohmaier, K; Visser, WH; Winner, P, 2004) |
"Rizatriptan was significantly more effective than non-triptans in the relief of migraine headaches for patients obtaining prescribed migraine medications from a retail pharmacy." | 2.71 | Migraine treatment with rizatriptan and non-triptan usual care medications: a pharmacy-based study. ( Adelman, J; Cady, R; Diamond, M; Hu, XH; Martin, V; Sajjan, S, 2004) |
" On experiencing moderate or severe migraine headaches, patients rated headache severity prior to dosing and at 30-minute intervals for 2 hours after dosing." | 2.69 | Rizatriptan (MAXALT) for the acute treatment of migraine and migraine recurrence. A placebo-controlled, outpatient study. Rizatriptan 022 Study Group. ( Block, G; Cutler, N; Gross, M; Jiang, K; Reines, S; Smith, B; Teall, J; Tuchman, M; Willoughby, E, 1998) |
"Rizatriptan wafer is a 5HT1B/1D agonist for use in the acute treatment of migraine." | 2.69 | Rizatriptan wafer--sublingual vs. placebo at the onset of acute migraine. ( Klapper, JA; O'Connor, S, 2000) |
"Rizatriptan (MK-462) is a potent 5HTID receptor agonist." | 2.68 | Double-blind, placebo-controlled, dose-finding study of rizatriptan (MK-462) in the acute treatment of migraine. ( Block, G; Ferrari, MD; Gijsman, H; Kramer, MS; Matzura-Wolfe, D; Polis, A; Sargent, J; Teall, J; Tuchman, M, 1997) |
"Migraine is a highly disabling condition for the individual and also has wide-reaching implications for society, healthcare services, and the economy." | 2.48 | Sumatriptan (intranasal route of administration) for acute migraine attacks in adults. ( Derry, CJ; Derry, S; Moore, RA, 2012) |
"Rizatriptan is a second-generation triptan marketed as 5 and 10 mg tablets and rapidly disintegrating wafer formulations." | 2.42 | A review of rizatriptan, a quick and consistent 5-HT1B/1D agonist for the acute treatment of migraine. ( Pascual, J, 2004) |
"Rizatriptan is a new, selective 5-HT1B/1D receptor agonist that is effective for treatment of migraine." | 2.41 | The use of rizatriptan in the treatment of acute, multiple migraine attacks. ( Saper, JR, 2000) |
"There exist increasing options for migraine treatment that may further improve the clinical effects of the older and newer triptans through early treatment of migraine at the stages of mild migraine pain, or even during the prodromal phase of the attack." | 2.41 | Acute treatment of migraine and the role of triptans. ( Freitag, FG, 2001) |
"Thus sumatriptan has become the de facto gold standard and will be thus employed here." | 2.40 | The scientific basis of medication choice in symptomatic migraine treatment. ( Goadsby, PJ, 1999) |
"Significantly, more patients taking rizatriptan achieved both PR and PF within 2 h after dosing than other oral triptans." | 1.34 | Times to pain relief and pain freedom with rizatriptan 10 mg and other oral triptans. ( Chen, Y; Hu, XH; Ma, L; Ng-Mak, DS; Solomon, G, 2007) |
"Migraine is a common disorder that costs US employers billions of dollars each year in missed workdays and reduced productivity." | 1.32 | Cost-effectiveness of almotriptan and rizatriptan in the treatment of acute migraine. ( Reeder, CE; Williams, P, 2003) |
"In the treatment of acute migraine, patients need a drug that provides convenient dosing and consistent effectiveness." | 1.31 | Rizatriptan. Convenience and consistency. ( Evans, RW, 2000) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (11.11) | 18.2507 |
2000's | 28 (77.78) | 29.6817 |
2010's | 4 (11.11) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Filla, SA | 1 |
Winter, MA | 1 |
Johnson, KW | 1 |
Bleakman, D | 1 |
Bell, MG | 1 |
Bleisch, TJ | 1 |
CastaƱo, AM | 1 |
Clemens-Smith, A | 1 |
del Prado, M | 1 |
Dieckman, DK | 1 |
Dominguez, E | 1 |
Escribano, A | 1 |
Ho, KH | 1 |
Hudziak, KJ | 1 |
Katofiasc, MA | 1 |
Martinez-Perez, JA | 1 |
Mateo, A | 1 |
Mathes, BM | 1 |
Mattiuz, EL | 1 |
Ogden, AM | 1 |
Phebus, LA | 1 |
Stack, DR | 1 |
Stratford, RE | 1 |
Ornstein, PL | 1 |
Cui, XP | 1 |
Ye, JX | 1 |
Lin, H | 1 |
Mu, JS | 1 |
Lin, M | 1 |
Freitag, F | 1 |
Diamond, M | 2 |
Diamond, S | 1 |
Janssen, I | 1 |
Rodgers, A | 3 |
Skobieranda, F | 3 |
Evans, RW | 1 |
Cady, RK | 2 |
Vause, CV | 1 |
Ho, TW | 2 |
Bigal, ME | 3 |
Durham, PL | 1 |
Savi, L | 1 |
Omboni, S | 1 |
Lisotto, C | 1 |
Zanchin, G | 1 |
Ferrari, MD | 3 |
Zava, D | 1 |
Pinessi, L | 1 |
Seeburger, JL | 1 |
Winner, P | 2 |
MacGregor, A | 1 |
Valade, D | 1 |
Ge, Y | 1 |
Zhang, Y | 1 |
Hustad, CM | 3 |
Strickler, N | 1 |
Schaefer, E | 1 |
Connor, KM | 1 |
Derry, CJ | 1 |
Derry, S | 1 |
Moore, RA | 2 |
Maizels, M | 1 |
Jamieson, D | 1 |
Cutrer, FM | 1 |
Goldstein, J | 1 |
Dayno, J | 1 |
Hu, XH | 3 |
Major, PW | 1 |
Grubisa, HS | 1 |
Thie, NM | 1 |
Williams, P | 1 |
Reeder, CE | 1 |
Pascual, J | 1 |
Krymchantowski, AV | 2 |
Visser, WH | 1 |
Strohmaier, K | 1 |
Klipfel, M | 1 |
Peng, Y | 1 |
McCarroll, K | 1 |
Cady, R | 3 |
Lewis, D | 1 |
Nett, R | 2 |
Martin, V | 2 |
Adelman, J | 1 |
Sajjan, S | 1 |
Morillo, LE | 1 |
Mauskop, A | 1 |
Ramsey, KE | 2 |
Tfelt-Hansen, P | 1 |
Iversen, HK | 1 |
Filho, PF | 1 |
Mannix, LK | 1 |
Loder, E | 1 |
Mueller, L | 1 |
Ng-Mak, DS | 1 |
Chen, Y | 1 |
Ma, L | 1 |
Solomon, G | 1 |
Misra, UK | 1 |
Kalita, J | 1 |
Yadav, RK | 1 |
Gijsman, H | 1 |
Kramer, MS | 1 |
Sargent, J | 1 |
Tuchman, M | 2 |
Matzura-Wolfe, D | 1 |
Polis, A | 1 |
Teall, J | 2 |
Block, G | 2 |
Cutler, N | 1 |
Gross, M | 1 |
Willoughby, E | 1 |
Smith, B | 1 |
Jiang, K | 1 |
Reines, S | 1 |
Deleu, D | 2 |
Hanssens, Y | 2 |
Goadsby, PJ | 3 |
Scholz, M | 1 |
Klapper, JA | 1 |
O'Connor, S | 1 |
Saper, JR | 1 |
Oldman, AD | 1 |
Smith, LA | 1 |
McQuay, HJ | 1 |
Roon, KI | 1 |
Lipton, RB | 1 |
Freitag, FG | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Correlation of Calcitonin Gene-Related Peptide (CGRP) Levels in Saliva With the Evolution of an Attack of Migraine[NCT00772473] | 34 participants (Actual) | Observational | 2008-02-29 | Completed | |||
Calcitonin Gene-related Peptide (CGRP) Levels in the Pathogenesis of Chronic Migraine[NCT01071096] | Phase 4 | 20 participants (Actual) | Interventional | 2010-06-30 | Completed | ||
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Crossover Trial to Evaluate the Efficacy and Tolerability of Rizatriptan 10 mg ODT for the Treatment of Acute Migraine in Patients on Topiramate for Migraine Prophylaxis[NCT00812006] | Phase 3 | 108 participants (Actual) | Interventional | 2009-03-24 | Completed | ||
A Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Examine the Efficacy of Rizatriptan 10 mg Tablet Administered Early During a Migraine Attack While the Pain is Mild[NCT00095004] | Phase 3 | 167 participants (Actual) | Interventional | 2004-10-21 | Completed | ||
A Multicenter, Double-Blind, Randomized, Parallel, Placebo-Controlled Study to Examine the Efficacy of Rizatriptan 10 mg Tablet Administered Early During a Migraine Attack While the Pain is Mild[NCT00092963] | Phase 3 | 529 participants (Actual) | Interventional | 2004-08-17 | Completed | ||
A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo Controlled Study to Evaluate the Efficacy and Tolerability of Rizatriptan 10 mg Tablets for the Treatment of Menstrual Migraine[NCT00111722] | Phase 3 | 393 participants (Actual) | Interventional | 2005-05-27 | Completed | ||
A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo Controlled Study to Evaluate the Efficacy and Tolerability of Rizatriptan 10 mg Tablets for the Treatment of Menstrual Migraine[NCT00111709] | Phase 3 | 393 participants (Actual) | Interventional | 2005-05-27 | Completed | ||
A Randomized, Triple-Blind, Double-Dummy, Placebo-Controlled, Parallel Groups, Outpatient Study to Examine the Safety and Efficacy of MK0462 10 mg p.o. and MK0462 5 mg p.o. for the Treatment of Acute Migraine and Migraine Recurrence[NCT00897949] | Phase 3 | 1,473 participants (Actual) | Interventional | 1995-03-31 | Completed | ||
Effects of Myofascial Trigger Points Therapy in Migraine.[NCT05646160] | 100 participants (Anticipated) | Interventional | 2018-01-15 | Recruiting | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Baseline number of headache days per month collected historically at screening. Post-treatment number of headache days collected per month via diary. (NCT01071096)
Timeframe: Baseline (collected historically at screening) versus (vs.) Month (Mo) 1, Mo 2, Mo 3, Mo 4, Mo 5, Mo 6, and Mo 7
Intervention | days (Mean) | ||||||
---|---|---|---|---|---|---|---|
Baseline vs. Month 1 | Baseline vs. Month 2 | Baseline vs. Month 3 | Baseline vs. Month 4 | Baseline vs. Month 5 | Baseline vs. Month 6 | Baseline vs. Month 7 | |
Group A | -7.61 | -9.72 | -10.06 | -9.50 | -8.94 | -9.50 | -6.50 |
Group B | -6.67 | -5.22 | -5.22 | -6.89 | -6.33 | -9.22 | -4.56 |
Baseline number of headache days per month collected historically at screening. Post-treatment number of headache days collected per month via diary. (NCT01071096)
Timeframe: Baseline (collected historically at screening) vs. Mo 1, Mo 1 vs. Mo 2, Mo 2 vs. Mo 3, Mo 3 vs. Mo 4, Mo 4 vs. Mo 5, Mo 5 vs. Mo 6, and Mo 6 vs. Mo 7
Intervention | days (Mean) | ||||||
---|---|---|---|---|---|---|---|
Baseline vs. Mo 1 | Mo 1 vs. Mo 2 | Mo 2 vs. Mo 3 | Mo 3 vs. Mo 4 | Mo 4 vs. Mo 5 | Mo 5 vs. Mo 6 | Mo 6 vs. M 7 | |
Group A | -7.61 | -2.11 | -0.33 | 0.56 | 0.56 | -0.56 | 3.00 |
Group B | -6.67 | 1.44 | 0.00 | -1.67 | 0.56 | -2.89 | 4.67 |
Only cytokines with a mean densimetric value 1.65 times the background grey value in a minimum of 3 patients were considered detectable. These are reported below. Values normalized to positive control array spots after background subtraction: C5/C5a, CD40 Ligand, Granulocyte Colony Stimulating Factor (G-CSF), Growth Regulated Oncogene(GRO)-alpha, Soluble Intercellular Adhesion Molecule (sICAM)-1, Interferon gamma (IFN-y), Interleukin(IL)-1alpha, 1beta, 1ra, 8, 16, 17E, & 23, Interferon Gamma-Induced Protein 10 (IP-10), Interferon-inducible T cell alpha chemoattractant (I-TAC), Macrophage Migration Inhibitory Factor (MIF), Serpin E1, and Regulated Upon Activation Normal T-cell Expressed (RANTES) (NCT01071096)
Timeframe: For OnabotulinumtoxinA and Saline treatment months 1, 2 and 3 at Baseline level (inter-ictal) and at onset of headache that is one degree worse than Baseline level and that will be treated with acute therapy
Intervention | Florescent Units (FU) (Mean) | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
C5/C5a | CD40 Ligand | G-CSF | GROa | sICAM-1 | IFN-y | IL-1alpha | IL-1beta | IL-1ra | IL-8 | IL-16 | IL-17E | IL-23 | IP-10 | I-TAC | MIF | Serpin E1 | RANTES | |
Month 1 vs. Month 3 Non-Responders | 3.26 | 1.22 | 1.34 | 0.73 | 1.51 | 1.63 | 0.81 | 1.03 | 1.30 | 2.28 | 1.10 | 1.45 | 2.61 | 3.11 | 3.65 | 1.24 | 3.16 | 1.24 |
Month 1 vs. Month 3 Responders | 1.03 | 0.91 | 1.07 | 1.05 | 3.99 | 0.91 | 0.86 | 1.15 | 0.88 | 4.38 | 0.98 | 1.28 | 0.93 | 1.55 | 0.67 | 0.80 | 0.76 | 1.14 |
Month 1 vs. Saline Non-Responders | 1.01 | 1.26 | 0.93 | 3.18 | 0.61 | 0.80 | 2.88 | 1.12 | 2.02 | 1.70 | 2.07 | 1.02 | 1.80 | 0.95 | 0.28 | 9.55 | 0.70 | 0.77 |
Month 1 vs. Saline Responders | 1.38 | 1.09 | 0.92 | 1.34 | 2.60 | 1.29 | 2.30 | 1.63 | 1.13 | 1.61 | 0.91 | 0.86 | 2.45 | 1.32 | 1.40 | 3.71 | 0.98 | 0.95 |
Month 3 vs. Saline Non-Responders | 1.61 | 1.31 | 0.99 | 1.81 | 2.00 | 1.92 | 2.14 | 0.51 | 1.90 | 1.22 | 1.97 | 0.42 | 1.69 | 2.76 | 0.94 | 8.66 | 0.90 | 0.91 |
Month 3 vs. Saline Responders | 1.39 | 0.98 | 0.85 | 1.40 | 5.99 | 1.29 | 1.50 | 1.38 | 0.96 | 2.71 | 0.75 | 1.59 | 1.06 | 0.86 | 1.01 | 2.71 | 0.70 | 0.93 |
CGRP Level collected each month when subject did not have a headache or was at lowest pain level of headache that month. (NCT01071096)
Timeframe: Baseline levels collected for OnabotulinumtoxinA and Saline treatment during Months 1 through 7
Intervention | pmol/mg total protein (Mean) | ||
---|---|---|---|
Treatment Month 1 | Treatment Month 2 | Treatment Month 3 | |
OnabotulinumtoxinA | 39.64 | 28.37 | 26.14 |
Saline | 40.79 | 39.14 | 50.63 |
Saliva samples collected at Baseline (at no headache or lowest level of headache), at headache attack directly before taking rescue medication and 2 hours after treating with rescue medication. (NCT01071096)
Timeframe: For OnabotulinumtoxinA and Saline treatment months 1, 2 and 3
Intervention | pmol/mg total protein (Mean) | ||||||||
---|---|---|---|---|---|---|---|---|---|
Treatment Month 1 - Baseline | Treatment Month 1 - Attack | Treatment Month 1 - 2 Hours Post | Treatment Month 2 - Baseline | Treatment Month 2 - Attack | Treatment Month 2 - 2 Hours Post | Treatment Month 3 - Baseline | Treatment Month 3 - Attack | Treatment Month 3 - 2 Hours Post | |
OnabotulinumtoxinA Non-Responders | 29.36 | 22.36 | 23.66 | 28.66 | 32.65 | 22.35 | 32.61 | 30.17 | 19.11 |
OnabotulinumtoxinA Responders | 52.36 | 27.94 | 61.55 | 59.89 | 60.14 | 39.13 | 51.33 | 73.18 | 54.04 |
Saline | 70.46 | 36.23 | 39.76 | 44.12 | 33.05 | 33.93 | 58.74 | 46.16 | 49.39 |
Level of functional disability was assessed on a paper diary by the participants. Level of functional disability was rated as: normal, mildly impaired, severely impaired, or unable to do activities, requires bedrest. Functional disability ratings was dichotomized to Normal and Not Normal (mildly impaired, severely impaired, or unable to do activities, requires bedrest) for analysis. (NCT00812006)
Timeframe: 2 hours post dose
Intervention | Attacks (Number) | |
---|---|---|
Resulting in NRFD at 2 hours post dose | Not resulting in NRFD at 2 hours post dose | |
Placebo | 16 | 77 |
Rizatriptan | 85 | 108 |
Headache pain severity, relative to the administration of study medication, was rated by the participants in a paper diary. Pain severity rating scale: 0 (no pain), 1 (mild pain), 2 (moderate pain), or 3 (severe pain). Pain freedom (PF) is defined as a reduction in headache severity from Grade 3/2 at baseline to Grade 0 (no pain) post dose. (NCT00812006)
Timeframe: 2 hours post dose
Intervention | Attacks (Number) | |
---|---|---|
Resulting in PF 2 hours post dose | Not resulting in PF 2 hours post dose | |
Placebo | 9 | 84 |
Rizatriptan | 74 | 119 |
Pain severity was rated by the participants in a paper diary. Pain severity rating scale : 0 (no pain), 1 (mild pain), 2 (moderate pain), or 3 (severe pain). Pain relief (PR) is defined as a reduction in headache severity from Grade 3/2 at baseline to Grade 1/0 post dose. (NCT00812006)
Timeframe: 2 hours post dose
Intervention | Attacks (Number) | |
---|---|---|
Resulting in PR at 2 hours post dose | Not resulting in PR at 2 hours post dose | |
Placebo | 21 | 72 |
Rizatriptan | 105 | 88 |
24-hour sustained pain relief (defined as pain relief at 2 hours post dose, with no administration of any rescue medication and with no occurrence of a moderate/severe headache during the respective period after dosing with the blinded study medication. (NCT00812006)
Timeframe: 2 - 24 hours post dose
Intervention | Attacks (Number) | |
---|---|---|
Resulting in SPR 2-24 hours post dose | Not resulting in SPR 2-24 hours post dose | |
Placebo | 12 | 81 |
Rizatriptan | 67 | 126 |
Patient satisfaction was assessed on a paper diary by the participants. Level of satisfaction was rated as: completely satisfied, very satisfied, somewhat satisfied, neither satisfied nor dissatisfied, somewhat dissatisfied, very dissatisfied, or completely dissatisfied. The overall 24-hour assessment of study medication was dichotomized to Satisfaction (completely satisfied, very satisfied, somewhat satisfied) and Non-satisfaction (neither satisfied nor dissatisfied, somewhat dissatisfied, very dissatisfied, or completely dissatisfied) for analysis. (NCT00812006)
Timeframe: 24 hours post dose
Intervention | Attacks (Number) | |
---|---|---|
Resulting in TS at 24 hours post dose | Not resulting in TS at 24 hours post dose | |
Placebo | 31 | 62 |
Rizatriptan | 117 | 76 |
Patients with no disability at 2 hours after the initial dose of test drug. Functional disability was subjectively rated on a scale from grade 0 to 3: Grade 0 - Normal, Grade 1 - Daily activities mildly impaired, Grade 2 - Daily activities severely impaired, Grade 3 - Unable to carry out daily activities, requires bedrest (NCT00897949)
Timeframe: 2 hours after initial dose of test drug
Intervention | Participants (Number) | |||
---|---|---|---|---|
Normal | Mildly Impaired | Severely Impaired | Requires Bedrest | |
Placebo | 54 | 118 | 53 | 75 |
Rizatriptan 10 mg | 209 | 148 | 45 | 52 |
Rizatriptan 5 mg | 175 | 160 | 56 | 66 |
Patients reporting pain free (defined as a reduction of headache severity to grade 0 [no pain]) at 2 hours after the initial dose of test drug. Pain severity was subjectively rated by patients on a scale from grade 0 to 3: Grade 0 - No headache, Grade 1 - Mild pain, Grade 2 - Moderate pain, Grade 3 - Severe pain. (NCT00897949)
Timeframe: 2 hours after initial dose of test drug
Intervention | Participants (Number) | |
---|---|---|
Reporting no pain | Reporting pain | |
Placebo | 30 | 272 |
Rizatriptan 10 mg | 193 | 262 |
Rizatriptan 5 mg | 150 | 307 |
Patients reporting pain relief 2 hours after treatment for headache recurrence (defined as the return of headache to grade 2 or 3 within 24 hours of the initial dose in patients who reported pain relief (grades 0 or 1) at 2 hours). (NCT00897949)
Timeframe: 2 hours after treatment for recurrence
Intervention | Participants (Number) | |
---|---|---|
Pain relief | No pain relief | |
Placebo / Rizatriptan 10 mg | 18 | 4 |
Placebo / Rizatriptan 5 mg | 12 | 5 |
Rizatriptan 10 mg / Placebo | 33 | 42 |
Rizatriptan 10 mg / Rizatriptan 10 mg | 53 | 12 |
Rizatriptan 5 mg / Placebo | 32 | 27 |
Rizatriptan 5 mg / Rizatriptan 5 mg | 39 | 16 |
Patients reporting pain relief (defined as a reduction of headache severity from grades 2/3 at baseline to 0/1) at 2 hours after the initial dose of test drug. Pain severity was subjectively rated by patients on a scale from grade 0 to 3: Grade 0 - No headache, Grade 1 - Mild pain, Grade 2 - Moderate pain, Grade 3 - Severe pain. (NCT00897949)
Timeframe: 2 hours after initial dose of test drug
Intervention | Participants (Number) | |
---|---|---|
Reporting pain relief | Not reporting pain relief | |
Placebo | 106 | 196 |
Rizatriptan 10 mg | 322 | 133 |
Rizatriptan 5 mg | 285 | 172 |
(NCT00897949)
Timeframe: 2 hours after initial dose of test drug
Intervention | Participants (Number) | |
---|---|---|
Used escape medication | Did not use escape medication | |
Placebo | 128 | 176 |
Rizatriptan 10 mg | 76 | 380 |
Rizatriptan 5 mg | 101 | 357 |
14 reviews available for rizatriptan and Acute Disease
Article | Year |
---|---|
Efficacy, safety, and tolerability of telcagepant in the treatment of acute migraine: a meta-analysis.
Topics: Acute Disease; Azepines; Calcitonin Gene-Related Peptide Receptor Antagonists; Humans; Imidazoles; M | 2015 |
Sumatriptan (intranasal route of administration) for acute migraine attacks in adults.
Topics: Acute Disease; Administration, Intranasal; Adult; Dihydroergotamine; Female; Humans; Male; Migraine | 2012 |
Triptans for treatment of acute pediatric migraine: a systematic literature review.
Topics: Acute Disease; Administration, Intranasal; Administration, Oral; Child; Clinical Trials as Topic; Hu | 2003 |
A review of rizatriptan, a quick and consistent 5-HT1B/1D agonist for the acute treatment of migraine.
Topics: Acute Disease; Administration, Oral; Clinical Trials as Topic; Drug Interactions; Humans; Migraine D | 2004 |
Migraine headache.
Topics: Acute Disease; Adult; Analgesics, Non-Narcotic; Anti-Inflammatory Agents, Non-Steroidal; Child; Dicl | 2003 |
[Triptanes in the treatment of migraine. A review based on three Cochrane reviews].
Topics: Acute Disease; Administration, Oral; Dose-Response Relationship, Drug; Humans; Migraine Disorders; P | 2006 |
Profiles of 5-HT 1B/1D agonists in acute migraine with special reference to second generation agents.
Topics: Acute Disease; Animals; Clinical Trials as Topic; Coronary Circulation; Coronary Vasospasm; Drug Des | 1999 |
The scientific basis of medication choice in symptomatic migraine treatment.
Topics: Acute Disease; Choice Behavior; Dose-Response Relationship, Drug; Humans; Indoles; Migraine Disorder | 1999 |
Current and emerging second-generation triptans in acute migraine therapy: a comparative review.
Topics: Acute Disease; Carbazoles; Humans; Indoles; Migraine Disorders; Oxazoles; Oxazolidinones; Piperidine | 2000 |
Rizatriptan in acute treatment of migraine: update on new comparative data.
Topics: Acute Disease; Clinical Trials as Topic; Humans; Migraine Disorders; Serotonin Receptor Agonists; Tr | 2000 |
The use of rizatriptan in the treatment of acute, multiple migraine attacks.
Topics: Acute Disease; Humans; Migraine Disorders; Recurrence; Serotonin Receptor Agonists; Triazoles; Trypt | 2000 |
Rizatriptan for acute migraine.
Topics: Acute Disease; Humans; Migraine Disorders; Randomized Controlled Trials as Topic; Serotonin Receptor | 2001 |
Oral triptans (serotonin 5-HT(1B/1D) agonists) in acute migraine treatment: a meta-analysis of 53 trials.
Topics: Acute Disease; Administration, Oral; Humans; Indoles; Migraine Disorders; Pyrrolidines; Randomized C | 2001 |
Acute treatment of migraine and the role of triptans.
Topics: Acute Disease; Blood Flow Velocity; Carbazoles; Clinical Trials as Topic; Drug Administration Routes | 2001 |
15 trials available for rizatriptan and Acute Disease
Article | Year |
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Efficacy and tolerability of coadministration of rizatriptan and acetaminophen vs rizatriptan or acetaminophen alone for acute migraine treatment.
Topics: Acetaminophen; Acute Disease; Adult; Aged; Analgesics, Non-Narcotic; Double-Blind Method; Drug Thera | 2008 |
Elevated saliva calcitonin gene-related peptide levels during acute migraine predict therapeutic response to rizatriptan.
Topics: Acute Disease; Adult; Biomarkers; Calcitonin Gene-Related Peptide; Drug Resistance; Female; Humans; | 2009 |
Elevated saliva calcitonin gene-related peptide levels during acute migraine predict therapeutic response to rizatriptan.
Topics: Acute Disease; Adult; Biomarkers; Calcitonin Gene-Related Peptide; Drug Resistance; Female; Humans; | 2009 |
Elevated saliva calcitonin gene-related peptide levels during acute migraine predict therapeutic response to rizatriptan.
Topics: Acute Disease; Adult; Biomarkers; Calcitonin Gene-Related Peptide; Drug Resistance; Female; Humans; | 2009 |
Elevated saliva calcitonin gene-related peptide levels during acute migraine predict therapeutic response to rizatriptan.
Topics: Acute Disease; Adult; Biomarkers; Calcitonin Gene-Related Peptide; Drug Resistance; Female; Humans; | 2009 |
Efficacy of frovatriptan in the acute treatment of menstrually related migraine: analysis of a double-blind, randomized, cross-over, multicenter, Italian, comparative study versus rizatriptan.
Topics: Acute Disease; Adolescent; Adult; Aged; Carbazoles; Cross-Over Studies; Double-Blind Method; Female; | 2011 |
Rizatriptan for treatment of acute migraine in patients taking topiramate for migraine prophylaxis.
Topics: Acute Disease; Adolescent; Adult; Aged; Disability Evaluation; Double-Blind Method; Female; Fructose | 2012 |
Real-world experiences in migraine therapy with rizatriptan.
Topics: Acute Disease; Adult; Female; Follow-Up Studies; Humans; Male; Middle Aged; Migraine Disorders; Pati | 2003 |
Rizatriptan versus rizatriptan plus rofecoxib versus rizatriptan plus tolfenamic acid in the acute treatment of migraine.
Topics: Acute Disease; Adolescent; Adult; Aged; Anti-Inflammatory Agents, Non-Steroidal; Cyclooxygenase Inhi | 2004 |
Rizatriptan 5 mg for the acute treatment of migraine in adolescents: results from a double-blind, single-attack study and two open-label, multiple-attack studies.
Topics: Acute Disease; Adolescent; Double-Blind Method; Female; Humans; Male; Migraine Disorders; Recurrence | 2004 |
Migraine treatment with rizatriptan and non-triptan usual care medications: a pharmacy-based study.
Topics: Acute Disease; Adolescent; Adult; Analgesics; Female; Humans; Male; Middle Aged; Migraine Disorders; | 2004 |
Efficacy of Rizatriptan 10 mg administered early in a migraine attack.
Topics: Acute Disease; Adult; Female; Humans; Male; Medical Records; Migraine Disorders; Patient Satisfactio | 2006 |
Efficacy of Rizatriptan 10 mg administered early in a migraine attack.
Topics: Acute Disease; Adult; Female; Humans; Male; Medical Records; Migraine Disorders; Patient Satisfactio | 2006 |
Efficacy of Rizatriptan 10 mg administered early in a migraine attack.
Topics: Acute Disease; Adult; Female; Humans; Male; Medical Records; Migraine Disorders; Patient Satisfactio | 2006 |
Efficacy of Rizatriptan 10 mg administered early in a migraine attack.
Topics: Acute Disease; Adult; Female; Humans; Male; Medical Records; Migraine Disorders; Patient Satisfactio | 2006 |
Rizatriptan vs. rizatriptan plus trimebutine for the acute treatment of migraine: a double-blind, randomized, cross-over, placebo-controlled study.
Topics: Acute Disease; Adolescent; Adult; Aged; Drug Combinations; Female; Gastrointestinal Agents; Gastropa | 2006 |
Rizatriptan for the acute treatment of ICHD-II proposed menstrual migraine: two prospective, randomized, placebo-controlled, double-blind studies.
Topics: Acute Disease; Adolescent; Adult; Analgesics; Comorbidity; Double-Blind Method; Female; Humans; Mens | 2007 |
Rizatriptan for the acute treatment of ICHD-II proposed menstrual migraine: two prospective, randomized, placebo-controlled, double-blind studies.
Topics: Acute Disease; Adolescent; Adult; Analgesics; Comorbidity; Double-Blind Method; Female; Humans; Mens | 2007 |
Rizatriptan for the acute treatment of ICHD-II proposed menstrual migraine: two prospective, randomized, placebo-controlled, double-blind studies.
Topics: Acute Disease; Adolescent; Adult; Analgesics; Comorbidity; Double-Blind Method; Female; Humans; Mens | 2007 |
Rizatriptan for the acute treatment of ICHD-II proposed menstrual migraine: two prospective, randomized, placebo-controlled, double-blind studies.
Topics: Acute Disease; Adolescent; Adult; Analgesics; Comorbidity; Double-Blind Method; Female; Humans; Mens | 2007 |
Rizatriptan vs. ibuprofen in migraine: a randomised placebo-controlled trial.
Topics: Acute Disease; Adult; Anti-Inflammatory Agents, Non-Steroidal; Female; Humans; Ibuprofen; Male; Migr | 2007 |
Double-blind, placebo-controlled, dose-finding study of rizatriptan (MK-462) in the acute treatment of migraine.
Topics: Acute Disease; Dose-Response Relationship, Drug; Double-Blind Method; Female; Humans; Logistic Model | 1997 |
Rizatriptan (MAXALT) for the acute treatment of migraine and migraine recurrence. A placebo-controlled, outpatient study. Rizatriptan 022 Study Group.
Topics: Acute Disease; Adolescent; Adult; Aged; Double-Blind Method; Female; Humans; Male; Middle Aged; Migr | 1998 |
Rizatriptan wafer--sublingual vs. placebo at the onset of acute migraine.
Topics: Acute Disease; Administration, Oral; Administration, Sublingual; Analgesics; Double-Blind Method; Fl | 2000 |
7 other studies available for rizatriptan and Acute Disease
Article | Year |
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Ethyl (3S,4aR,6S,8aR)-6-(4-ethoxycar- bonylimidazol-1-ylmethyl)decahydroiso-quinoline-3-carboxylic ester: a prodrug of a GluR5 kainate receptor antagonist active in two animal models of acute migraine.
Topics: Acute Disease; Administration, Oral; Animals; Biological Availability; Calcium; Carboxylic Acids; Ce | 2002 |
Rizatriptan. Convenience and consistency.
Topics: Acute Disease; Administration, Oral; Humans; Migraine Disorders; Serotonin Receptor Agonists; Tablet | 2000 |
Rizatriptan 5mg is not efficacious for migraine in adolescents.
Topics: Acute Disease; Adolescent; Humans; Migraine Disorders; Randomized Controlled Trials as Topic; Seroto | 2002 |
[New onset headache. Which patients should be sent for CT imaging?].
Topics: Acute Disease; Brain Diseases; Diagnosis, Differential; Drug Administration Schedule; Headache; Huma | 2002 |
Cost-effectiveness of almotriptan and rizatriptan in the treatment of acute migraine.
Topics: Acute Disease; Cost-Benefit Analysis; Decision Support Techniques; Female; Health Care Costs; Health | 2003 |
Times to pain relief and pain freedom with rizatriptan 10 mg and other oral triptans.
Topics: Acute Disease; Adult; Cross-Over Studies; Female; Humans; Male; Middle Aged; Migraine Disorders; Mul | 2007 |
Treatment options for acute migraine.
Topics: Acute Disease; Adult; Female; Humans; Migraine Disorders; Oxazolidinones; Patient Selection; Practic | 2000 |