drugset / Trial / NCT01708005
DIetary Supplements, Executive funcTions and Vitamin D (DIET-D)
Phase 2/3
Unknown
160 enrolled
University Hospital, Angers
NUTRISANTE · collabNantes University Hospital · collab
RandomizedParallel-groupQuadruple-blindPrevention
Summary
The purpose of this study is to compare the effect after 12 weeks of the oral intake of Lecitone®Se + 200UI/day of D3 vitamin with the effect of a placebo on changes in cognitive performance in Trial Making Test score part B (this test evaluate executive functions of mental flexibility) in older adults with Mild Cognitive Impairment (MCI).
Timeline
- Start
- 2012-11
- Primary completion
- 2014-11
- Completion
- 2014-11
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Cholecalciferol | Other / unclassified | 200 iu | Oral |
| Comparator | Lecitone®Se | Unknown | — | Oral |