Last updated: 11/07/2018 18:20:39
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study To Evaluate The Efficacy Of Oral Naratriptan (2.5mg) For The Treatment Of Migraine In Subjects Who Do Not Respond To Oral Sumatriptan (50mg)
Clinicaltrials.gov ID
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EudraCT ID
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EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study To Evaluate The Efficacy Of Oral Naratriptan (2.5mg) For The Treatment Of Migraine In Subjects Who Do Not Respond To Oral Sumatriptan (50mg)
Trial description: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study To Evaluate The Efficacy Of Oral Naratriptan (2.5mg) For The Treatment Of Migraine In Subjects Who Do Not Respond To Oral Sumatriptan (50mg)
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Abstract: Naratriptan is effective for the treatment of migraine headache in sumatriptan non responders. Stark, S MD, O'Quinn, S MD, McNeal, S MD, Pait, G MD, and Watson, C MD American Academy of Neurology 51st Annual Meeting 4/17/1999 Toronto, Canada
Abstract: Naratriptan is effective for the treatment of migraine headache in sumatriptan non responders. Stark, S MD, O'Quinn, S MD, McNeal, S MD, Putnam, G MD, and Watson, C MD 41st Annual Scientific Meeting of the American Association for the Study of Headache 6/11/1999 Boston, MA
Abstract: Naratriptan is effective for the treatment of migraine headache in sumatriptan non-responders. Spierings, E L H, Stark, S, O'Quinn, S, McNeal, S, Pait, G, and Watson, C 9th Congress of the International Headache Society 6/22/1999 Barcelona, Spain
Stark S; Naratriptan efficacy in migraineurs who respond poorly to oral sumatriptan: HEADACHE 2000;40(7)513-520.
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1998-30-06
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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