drugset / Trial / NCT04574713
Candesartan for Migraine Prevention:
Phase 2
Completed
450 enrolled
St. Olavs Hospital
Haukeland University Hospital · collabMolde Hospital · collabNordlandssykehuset HF · collabNorwegian University of Science and Technology · collabRikshospitalet University Hospital · collabSorlandet Hospital HF · collabTartu University Hospital · collabUllevaal University Hospital · collabUniversity Hospital of North Norway · collabUniversity Hospital, Akershus · collab
RandomizedParallel-groupTriple-blindPrevention
Summary
The main objective of this study is to see whether the favorable preventative effect of candesartan 16 mg per day in episodic migraine, that was found previously in two smaller randomized controlled cross-over studies, can be confirmed in a larger, multicenter, randomized controlled parallel group study. In addition it will be investigated whether 1) also a smaller dose of 8 mg is effective, and 2) whether the favorable side effect profile, seen in previous studies, can be confirmed, and whether it is even better with the smaller dose.
Timeline
- Start
- 2021-04-09
- Primary completion
- 2024-04-12
- Completion
- 2024-08-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Candesartan | Unknown | 8 mg | Oral |
| Subject | Candesartan | Unknown | 16 mg | Oral |