drugset / Trial / NCT03384329
Efficacy of Resveratrol in Depression
Phase 4
Completed
30 enrolled
Russian Academy of Medical Sciences
Russian Science Foundation · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
Patients with depression (target number - 60) receive resveratrol 500 mg or placebo (1:1) each morning daily for 1 month with primary outcome measures of the score change on depression rating scale HDRS-17 and change in SIRT1 activity in the blood measured 4 times over the study period (before, in the middle, after the intervention, and in 2 week follow up).
Timeline
- Start
- 2018-07-04
- Primary completion
- 2019-08-27
- Completion
- 2019-09-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Resveratrol | Small molecule | 500 mg | — |