Last updated: 11/07/2018 19:30:08
A randomised, double-blind, cross-over study to compare the efficacy and safety of sumatriptan 25mg suppository with cafergot suppository (2mg ergotamine tartrate, 100mg caffeine) (one suppository plus option of one additional suppository) in the acute treatment of migraine.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A randomised, double-blind, cross-over study to compare the efficacy and safety of sumatriptan 25mg suppository with cafergot suppository (2mg ergotamine tartrate, 100mg caffeine) (one suppository plus option of one additional suppository) in the acute treatment of migraine.
Trial description: A randomised, double-blind, cross-over study to compare the efficacy and safety of sumatriptan 25mg suppository with cafergot suppository (2mg ergotamine tartrate, 100mg caffeine) (one suppository plus option of one additional suppository) in the acute treatment of 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:
Sumatriptan suppositories for the acute treatment of migraine. s2b351 study group. Tepper, S. J., Cochran, A., Hobbs, S., and Woessner, M. Int J Clin Pract 1998; 52(1):31-5
Medical condition
Migraine Disorders
Product
sumatriptan
Collaborators
Not applicable
Study date(s)
N/A to Invalid Date
Type
Not applicable
Phase
3
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
Not applicable
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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