Clinical Trials Directory

Trials / Completed

CompletedNCT02904109

Influence of Triflusal on Cognitive Functions in Subjects Under Chronic Stress

Randomized Placebo Controlled Phase II Cross Over Study on the Influence of Triflusal on Cognitive Functions in Subjects Under Chronic Stress

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Prof. Dominique de Quervain, MD · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to investigate the effects of the eNOS activating agent triflusal on episodic memory and cognitive functions in participants under chronic stress.

Detailed description

Randomised, placebo controlled, double blind, cross-over design Primary study outcome is: Performance in a verbal memory task. Main secondary outcomes are: Performance in working memory and cognitive tasks and influence on mood, depression and anxiety and subjective memory impairment. Once daily oral administration of 600 mg triflusal and placebo mannitol for 8 days in a cross-over trial with a washout period of at least 14 days between the two periods. Each participant will take triflusal as well as placebo

Conditions

Interventions

TypeNameDescription
DRUGTriflusalOnce daily oral administration of 600 mg triflusal Disgren® for 8 days.
DRUGPlaceboOnce daily oral administration of placebo mannitol for 8 days.

Timeline

Start date
2016-09-13
Primary completion
2017-02-21
Completion
2017-02-28
First posted
2016-09-16
Last updated
2017-03-01

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT02904109. Inclusion in this directory is not an endorsement.