rizatriptan has been researched along with Addiction, Opioid in 1 studies
rizatriptan: structure given in first source; RN given refers to benzoate
Excerpt | Relevance | Reference |
---|---|---|
"In the moderate/severe migraine studies of 2068 individuals treated with rizatriptan, 284 (13." | 2.74 | Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis. ( Bigal, ME; Ho, TW; Rodgers, A, 2009) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ho, TW | 1 |
Rodgers, A | 1 |
Bigal, ME | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
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 Randomized, Triple-Blind, Placebo-Controlled, Outpatient Study to Examine the Safety and Efficacy of MK462 10 mg p.o. in the Treatment of Multiple Attacks of Migraine Headache[NCT00899379] | Phase 3 | 473 participants (Actual) | Interventional | 1995-04-30 | Completed | ||
A Randomized, Placebo-Controlled, Parallel-Groups, Outpatient Study to Examine the Safety, Tolerability, and Efficacy of Single Oral Doses of MK0462 5 mg, MK0462 10 mg, and Sumatriptan 100 mg for Acute Treatment of Migraine[NCT00898677] | Phase 3 | 1,268 participants (Actual) | Interventional | 1995-09-30 | 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 | ||
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 | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Patients reporting pain relief defined as a reduction of headache severity from grades 2 or 3 (moderate or severe) at baseline to grades 0 or 1 (no headache or mild) at 2 hours after initial dosing for the first migraine attack (NCT00899379)
Timeframe: 2 hours
Intervention | participants (Number) | |
---|---|---|
Reporting pain relief | Not reporting pain relief | |
Placebo | 30 | 52 |
Rizatriptan 10 mg | 246 | 74 |
Patients reporting pain relief defined as a reduction of headache severity from grades 2 or 3 (moderate or severe) to grades 0 or 1 (no headache or mild) at 2 hours after dosing for the fourth migraine attack (NCT00899379)
Timeframe: 2 hours
Intervention | Participants (Number) | |
---|---|---|
Reporting pain relief | Not reporting pain relief | |
Placebo | 31 | 26 |
Rizatriptan 10 mg | 190 | 65 |
Patients reporting pain relief defined as a reduction of headache severity from grades 2 or 3 (moderate or severe) to grades 0 or 1 (no headache or mild) at 2 hours after dosing for the second migraine attack (NCT00899379)
Timeframe: 2 hours
Intervention | Participants (Number) | |
---|---|---|
Reporting pain relief | Not reporting pain relief | |
Placebo | 27 | 46 |
Rizatriptan 10 mg | 228 | 63 |
Patients reporting pain relief defined as a reduction of headache severity from grades 2 or 3 (moderate or severe) to grades 0 or 1 (no headache or mild) at 2 hours after dosing for the third migraine attack (NCT00899379)
Timeframe: 2 hours
Intervention | Participants (Number) | |
---|---|---|
Reporting pain relief | Not reporting pain relief | |
Placebo | 21 | 54 |
Rizatriptan 10 mg | 207 | 52 |
Patients with no functional disability measured by the level of impairment to daily activities at 2 hours after treatment. Each patient rated functional disability on a 4-grade scale (0 = no functional disability; 1 = daily activities mildly impaired; 2 = daily activities severely impaired; 3 = unable to carry out daily activities, requires bed rest). (NCT00898677)
Timeframe: 2 hours after dose
Intervention | Participants (Number) | |||
---|---|---|---|---|
No functional disability | Mildly impaired | Severely impaired | Required bed rest | |
Placebo | 31 | 59 | 33 | 36 |
Rizatriptan 10 mg | 160 | 123 | 60 | 42 |
Rizatriptan 5 mg | 52 | 62 | 27 | 23 |
Sumatriptan 100 mg | 126 | 142 | 67 | 52 |
Patients who recorded the presence or absence of nausea 2 hours after dose (NCT00898677)
Timeframe: 2 hours after dose
Intervention | participants (Number) | |
---|---|---|
2-hour Nausea | No 2-hour Nausea | |
Placebo | 68 | 91 |
Rizatriptan 10 mg | 95 | 290 |
Rizatriptan 5 mg | 37 | 127 |
Sumatriptan 100 mg | 128 | 259 |
Patients pain free (defined as a reduction of headache severity to grade 0 [no pain]) at 2 hours after treatment. Each patient rated headache severity on a 4-point scale (0 = no headache; 1 = mild pain; 2 = moderate pain; 3 = severe pain). (NCT00898677)
Timeframe: 2 hours after dose
Intervention | Participants (Number) | |
---|---|---|
2-hour Pain freedom | No 2-hour pain freedom | |
Placebo | 15 | 139 |
Rizatriptan 10 mg | 155 | 230 |
Rizatriptan 5 mg | 41 | 123 |
Sumatriptan 100 mg | 127 | 260 |
Patients reporting pain relief defined as a reduction of headache severity from grades 2 or 3 (moderate or severe pain) at baseline to grades 0 or 1 (no headache or mild pain) at 2 hours after treatment (NCT00898677)
Timeframe: 2 hours after dose
Intervention | Participants (Number) | |
---|---|---|
2-hour pain relief | No 2-hour pain relief | |
Placebo | 64 | 95 |
Rizatriptan 10 mg | 258 | 127 |
Rizatriptan 5 mg | 99 | 65 |
Sumatriptan 100 mg | 239 | 148 |
Patients reporting time to relief defined as the first time point at which a patient reported headache severity grade 1 or 0 (mild pain or no headache) within 2 hours after dose (NCT00898677)
Timeframe: within 2 hours after dose
Intervention | Participants (Number) | |
---|---|---|
First pain relief within 2 hrs | Pain relief did not occur within 2 hrs | |
Placebo | 72 | 87 |
Rizatriptan 10 mg | 265 | 120 |
Rizatriptan 5 mg | 102 | 62 |
Sumatriptan 100 mg | 247 | 140 |
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 |
1 trial available for rizatriptan and Addiction, Opioid
Article | Year |
---|---|
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |
Impact of recent prior opioid use on rizatriptan efficacy. A post hoc pooled analysis.
Topics: Adult; Dose-Response Relationship, Drug; Female; Humans; Male; Migraine Disorders; Opioid-Related Di | 2009 |