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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02478034
Other study ID # WI-CO-2
Secondary ID
Status Completed
Phase N/A
First received June 11, 2015
Last updated March 4, 2016
Start date May 2015
Est. completion date March 2016

Study information

Verified date March 2016
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

In this study the effects of mineralocorticoid stimulation on social cognition will be investigated in healthy young individuals.


Description:

80 healthy young individuals (40 females and 40 male) will be recruited an randomized to either placebo or 0.4 mg Fludrocortison before testing. Tasks will on emotion recognition, Task Switch, visual spacial memory and decision making will be conducted.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- free of medication

- age 18 - 30

Exclusion Criteria:

- any medication

- severe illness

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Fludrocortisone
effects of fludrocortisone on cognition compared to placebo

Locations

Country Name City State
Germany Charite University Berlin

Sponsors (1)

Lead Sponsor Collaborator
Charite University, Berlin, Germany

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary social cognition computer based tests: emotion recognition 25 min No
Secondary memory computer based test on visuospacial memory 20 min No
Secondary decision making computer based tests: BART 25 min No
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