Last updated: 11/07/2018 18:18:14
A randomized, double-blind, placebo-controlled, parallel group evaluation of oral naratriptan 1 mg twice daily asprophylactic treatment for menstrually-associated migraine.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
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EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A randomized, double-blind, placebo-controlled, parallel group evaluation of oral naratriptan 1 mg twice daily asprophylactic treatment for menstrually-associated migraine.
Trial description: A randomized, double-blind, placebo-controlled, parallel group evaluation of oral naratriptan 1 mg twice daily asprophylactic treatment for menstrually-associated migraine.
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 for intermittent prophylaxis for menstrually-associated migraine: an analysis of migraine-free days. Diamond, M., Aurora, S., Ames, M., and Shackelford, S. 45th Annual Scientific Meeting of the American Headache Society (AHS) 6/19/2003 Chicago, IL; USA
Mannix LK et al. Efficacy and tolerability of naratriptan for short-term prevention of menstrually related migraine: data from two randomized, double-blind, placebo-controlled studies. Headache 2007;47:1037-1049.
Nett R, Mannix L, Landy S et al. Randomised, Double-Blind, Placebo-Controlled, Parallel Group Evaluation of Oral Naratriptan 1mg Twice Daily as Prophylactic Treatment for Menstrually-Associated Migraine. Platform Presentation at the 55th Annual Meeting of the American Academy of Neurology, Honolulu, HA. March 29-April 5th, 2003. [S15.006].
Medical condition
Migraine Disorders
Product
naratriptan
Collaborators
Not applicable
Study date(s)
December 1999 to December 2000
Type
Not applicable
Phase
4
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
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
2000-20-12
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
Not applicable
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