Last updated: 11/07/2018 19:33:52
A randomised, multi-centre, open-label, crossover study to evaluate patient preference for sumatriptan 50mg and 100mg, naratriptan 2.5mg, rizatriptan 10mg and zolmitriptan 2.5mg tablets 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, multi-centre, open-label, crossover study to evaluate patient preference for sumatriptan 50mg and 100mg, naratriptan 2.5mg, rizatriptan 10mg and zolmitriptan 2.5mg tablets in the acute treatment of migraine.
Trial description: A randomised, multi-centre, open-label, crossover study to evaluate patient preference for sumatriptan 50mg and 100mg, naratriptan 2.5mg, rizatriptan 10mg and zolmitriptan 2.5mg tablets 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:
Dahlöf C, Jones M, Davis K, Loftus J, Salonen R. A comparison of preference for and efficacy of tablet formulations of sumatriptan (50 mg and 100 mg), naratriptan (2.5 mg), rizatriptan (10 mg), and zolmitriptan (2.5 mg) in the acute treatment of migraine. J Headache Pain (2004) 5:115–22.
Triptan efficacy and preference: results of a randomized, multi-centre, open-label, crossover study of sumatriptan, naratriptan, rizatriptan, and zolmitriptan tablets in acute treatment of migraine. Dahlof, C, Fabri, M, Loftus, J, Jones, M, Mansback, H, and Scott, A 10th Congress of the International Headache Society and the American Association for the Study of Headache 43rd Annual Scientific Meeting 6/29/2001 New York, NY; USA
Medical condition
Migraine Disorders
Product
sumatriptan
Collaborators
Not applicable
Study date(s)
November 1999 to August 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
2000-25-08
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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