oxybutynin has been researched along with Abdominal Migraine in 12 studies
oxybutynin: RN given refers to parent cpd
oxybutynin : A racemate comprising equimolar amounts of (R)-oxybutynin and esoxybutynin. An antispasmodic used for the treatment of overactive bladder.
Excerpt | Relevance | Reference |
---|---|---|
" Systemic adverse events were consistent with previous triptan trials, and included dizziness, paresthesia, muscle tightness, and nausea, all of which occurred in < 5% of patients in any group." | 2.87 | Randomized, double-blind, placebo-controlled, parallel-group, multi-center study of the safety and efficacy of ADAM zolmitriptan for the acute treatment of migraine. ( Brandes, JL; Kellerman, DJ; Kudrow, DB; Schmidt, PC; Spierings, EL; Tepper, SJ; Weintraub, J, 2018) |
" Migraine-associated gastroparesis can impair absorption and reduce bioavailability of oral migraine medications and thereby reduce and delay therapeutic efficacy." | 2.77 | Twelve-month tolerability and efficacy study of NP101, the sumatriptan iontophoretic transdermal system. ( Goldstein, J; Pierce, MW; Pugach, N; Silberstein, S; Singer, R; Smith, TR, 2012) |
"One third of patients who experience migraine-related nausea report that this symptom interferes with their ability to take oral medications." | 2.77 | A sumatriptan iontophoretic transdermal system for the acute treatment of migraine. ( Goldstein, J; Griesser, J; Pierce, M; Pugach, N; Sebree, T; Smith, TR, 2012) |
"Many migraineurs awake early in the morning with their attack progressing and already associated with nausea and vomiting." | 2.46 | Innovative delivery systems for migraine: the clinical utility of a transdermal patch for the acute treatment of migraine. ( Freitag, F; Pearlman, SH; Rapoport, AM, 2010) |
" Pharmacokinetic studies showed that the ADAM 1." | 1.48 | Pharmacokinetics and Skin Tolerability of Intracutaneous Zolmitriptan Delivery in Swine Using Adhesive Dermally Applied Microarray. ( Ameri, M; Diep, AN; Hochart, G; Lewis, H; Nguyen, J; Queja, A, 2018) |
" As of 2018, the FDA Adverse Event Reporting System public dashboard lists a total of 2889 reports of safety problems with the patch, 904 of which were classified as serious." | 1.48 | Safety Problems With a Transdermal Patch for Migraine: Lessons From the Development, Approval, and Marketing Process. ( Burch, RC; Loder, EW; Rayhill, M, 2018) |
"Because migraine attacks can be disabling, with many patients unable to perform their usual activities, it is important for prescribers and their patients to be confident that they will be able to assemble and apply sumatriptan TDS in the middle of an attack." | 1.40 | Sumatriptan transdermal system can be correctly assembled and applied during migraine attacks. ( Foster, S; Jennings, C; Meadows, KP; O'Neill, C; Pierce, M, 2014) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 12 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Spierings, EL | 1 |
Brandes, JL | 1 |
Kudrow, DB | 1 |
Weintraub, J | 1 |
Schmidt, PC | 1 |
Kellerman, DJ | 1 |
Tepper, SJ | 1 |
Nguyen, J | 1 |
Lewis, H | 1 |
Queja, A | 1 |
Diep, AN | 1 |
Hochart, G | 1 |
Ameri, M | 1 |
Loder, EW | 1 |
Rayhill, M | 1 |
Burch, RC | 1 |
Meadows, KP | 1 |
Pierce, M | 2 |
O'Neill, C | 1 |
Foster, S | 1 |
Jennings, C | 1 |
Tepper, DE | 1 |
Aschenbrenner, DS | 1 |
Rapoport, AM | 1 |
Freitag, F | 1 |
Pearlman, SH | 1 |
Tfelt-Hansen, P | 1 |
Almén-Christensson, A | 1 |
Hammar, M | 1 |
Lindh-Åstrand, L | 1 |
Landtblom, AM | 1 |
Brynhildsen, J | 1 |
Smith, TR | 2 |
Goldstein, J | 2 |
Singer, R | 1 |
Pugach, N | 2 |
Silberstein, S | 1 |
Pierce, MW | 1 |
Griesser, J | 1 |
Sebree, T | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Randomized, Double-blind, Multi-center, Parallel-group, Dose-ranging Comparison of the Safety and Efficacy of the ZP-Zolmitriptan Intracutaneous Microneedle Systems to Placebo for the Acute Treatment of Migraine[NCT02745392] | Phase 2/Phase 3 | 365 participants (Actual) | Interventional | 2016-06-30 | Completed | ||
[NCT00204074] | Phase 2/Phase 3 | 0 participants | Interventional | 2001-10-31 | Active, not recruiting | ||
An Open-Label Study to Evaluate the Safety of NP101, a Sumatriptan Iontophoretic Transdermal Patch, in the Treatment of Acute Migraine Over 12 Months[NCT00792103] | Phase 3 | 198 participants (Actual) | Interventional | 2009-01-31 | Completed | ||
The Efficacy and Tolerability of NP101, a Sumatriptan Iontophoretic Transdermal Patch, in the Treatment of Acute Migraine: A Randomized, Double-Blind, Placebo-Controlled Study[NCT00724815] | Phase 3 | 530 participants (Actual) | Interventional | 2009-01-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
The proportion of subjects with freedom from the subject's pre-specified most bothersome symptom at 2 hours is one of two parts of the co-primary efficacy endpoint. This endpoint will be evaluated separately but both endpoints have to be met statistically for the study to be considered a success. (NCT02745392)
Timeframe: 2 hours
Intervention | Participants (Count of Participants) |
---|---|
Placebo | 33 |
ZP-Zolmitriptan 1 mg | 45 |
ZP-Zolmitriptan 1.9 mg | 44 |
ZP-Zolmitriptan 3.8 mg | 56 |
Pain Freedom at 2 hours post study drug administration is one of the co-primary endpoints. Subjects were queried via their eDiary about their level of migraine pain (none, mild, moderate, or severe) at various intervals post-dose. Subjects who answered none at 2 hours post study drug were considered pain free at 2 hours. (NCT02745392)
Timeframe: 2 hours
Intervention | Participants (Count of Participants) |
---|---|
Placebo | 11 |
ZP-Zolmitriptan 1 mg | 24 |
ZP-Zolmitriptan 1.9 mg | 23 |
ZP-Zolmitriptan 3.8 mg | 34 |
Nausea free at two hours after patch activation. (NCT00792103)
Timeframe: 2 hours
Intervention | participants (Number) |
---|---|
NP101 | 143 |
Headache pain relief (no pain or mild headache pain) at two hours post activation of NP101. (NCT00792103)
Timeframe: 2 hours
Intervention | participants (Number) |
---|---|
NP101 | 105 |
Phonophobia free at two hours after patch activation. (NCT00792103)
Timeframe: 2 hours
Intervention | participants (Number) |
---|---|
NP101 | 109 |
Photophobia free at two hours after patch activation. (NCT00792103)
Timeframe: 2 hours
Intervention | participant (Number) |
---|---|
NP101 | 97 |
For each patch application, subjects performed a self-examination of skin irritation using a 5-point scale (0=no redness; 1=minimal skin redness; 2=moderate skin redness with sharp borders; 3=intense skin redness with or without swelling; 4=intense skin redness with blisters or broken skin). (NCT00792103)
Timeframe: 24 hours post patch activation
Intervention | scores on a scale (Mean) |
---|---|
NP101 | 1.0 |
Number of subjects who were nausea free and who had not received any rescue medication before their two-hour assessment. (NCT00724815)
Timeframe: 2 hours post patch activation
Intervention | participants (Number) |
---|---|
NP101 Patch | 189 |
Placebo Patch | 144 |
Subjects whose headache severity score equaled zero (0) two hours post patch activation and who had not received any rescue medication before their two-hour assessment. (NCT00724815)
Timeframe: 2 hours post patch activation
Intervention | participants (Number) |
---|---|
NP101 Patch | 40 |
Placebo Patch | 21 |
Subjects who were phonophobia free and who had not received any rescue medication before their two-hour assessment. (NCT00724815)
Timeframe: 2 hours post patch activation
Intervention | participants (Number) |
---|---|
NP101 Patch | 125 |
Placebo Patch | 89 |
Subjects who were photophobia free and who had not received any rescue medication before their two-hour assessment. (NCT00724815)
Timeframe: 2 hours post patch activation
Intervention | participants (Number) |
---|---|
NP101 Patch | 116 |
Placebo Patch | 83 |
2 reviews available for oxybutynin and Abdominal Migraine
Article | Year |
---|---|
Sumatriptan iontophoretic patch for migraine.
Topics: Humans; Iontophoresis; Migraine Disorders; Serotonin 5-HT1 Receptor Agonists; Sumatriptan; Transderm | 2014 |
Innovative delivery systems for migraine: the clinical utility of a transdermal patch for the acute treatment of migraine.
Topics: Clinical Trials as Topic; Drug Administration Routes; Female; Gastroparesis; Humans; Iontophoresis; | 2010 |
4 trials available for oxybutynin and Abdominal Migraine
Article | Year |
---|---|
Randomized, double-blind, placebo-controlled, parallel-group, multi-center study of the safety and efficacy of ADAM zolmitriptan for the acute treatment of migraine.
Topics: Administration, Cutaneous; Adult; Double-Blind Method; Female; Humans; Male; Middle Aged; Migraine D | 2018 |
Prevention of menstrual migraine with perimenstrual transdermal 17-β-estradiol: a randomized, placebo-controlled, double-blind crossover study.
Topics: Administration, Cutaneous; Adult; Cross-Over Studies; Double-Blind Method; Drug Administration Sched | 2011 |
Twelve-month tolerability and efficacy study of NP101, the sumatriptan iontophoretic transdermal system.
Topics: Administration, Cutaneous; Adolescent; Adult; Aged; Chemistry, Pharmaceutical; Female; Follow-Up Stu | 2012 |
A sumatriptan iontophoretic transdermal system for the acute treatment of migraine.
Topics: Adult; Analgesics; Double-Blind Method; Female; Humans; Iontophoresis; Male; Migraine Disorders; Sum | 2012 |
6 other studies available for oxybutynin and Abdominal Migraine
Article | Year |
---|---|
Pharmacokinetics and Skin Tolerability of Intracutaneous Zolmitriptan Delivery in Swine Using Adhesive Dermally Applied Microarray.
Topics: Administration, Cutaneous; Animals; Biological Availability; Drug Delivery Systems; Equipment Design | 2018 |
Safety Problems With a Transdermal Patch for Migraine: Lessons From the Development, Approval, and Marketing Process.
Topics: Adverse Drug Reaction Reporting Systems; Burns, Chemical; Cicatrix; Clinical Trials as Topic; Drug A | 2018 |
Sumatriptan transdermal system can be correctly assembled and applied during migraine attacks.
Topics: Adolescent; Adult; Drug Delivery Systems; Female; Follow-Up Studies; Humans; Iontophoresis; Male; Mi | 2014 |
A sumatriptan patch (Zecuity) for migraine.
Topics: Adult; Double-Blind Method; Humans; Migraine Disorders; Randomized Controlled Trials as Topic; Serot | 2015 |
Sumatriptan Patch is Temporarily Suspended.
Topics: Administration, Cutaneous; Burns; Drug-Related Side Effects and Adverse Reactions; Humans; Migraine | 2016 |
Low efficacy of transdermal sumatriptan in migraine.
Topics: Humans; Migraine Disorders; Randomized Controlled Trials as Topic; Sumatriptan; Transdermal Patch; T | 2011 |