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NCT03353441

Effects of Microencapsulated Sublingual Glycine (Bidicin) on Cognitive Performance in Healthy Men After an Acute Stressor

Completed NA Last updated 26 July 2018
What this trial tests

NA trial testing Microencapsulated Sublingual Glycine (MSG) in Healthy in 90 participants. Completed in 15 June 2018.

Timeline
15 November 2017
Primary endpoint
15 March 2018
15 June 2018

Quick facts

Lead sponsorDaacro
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment90
Start date15 November 2017
Primary completion15 March 2018
Estimated completion15 June 2018
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Daacro

Who can join

Adults 18 to 40, male only, with Healthy or Stress, Psychological. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to assess whether intake of Glycine (MSG) leads to an increase of cognitive performance after an acute stressor compared to placebo. One group will receive verum, one group placebo and one group will not receive any intervention. Cognitive testing will be performed in connection with the Trier Social Stress Test (TSST).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Daacro trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03353441.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing