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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02478021
Other study ID # WI-CO-1
Secondary ID
Status Completed
Phase N/A
First received June 11, 2015
Last updated June 18, 2015
Start date September 2014
Est. completion date May 2015

Study information

Verified date June 2015
Source Charite University, Berlin, Germany
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

The effects of hydrocortisone on cognition will be investigated.


Description:

80 healthy young individuals (40 females and 40 male) will be recruited an randomized to either placebo or 10 mg hydrocortisone before testing. Tasks will on emotion recognition, memory and cognitive flexibilty will be conducted.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date May 2015
Est. primary completion date May 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- age 18 - 30

- medication free

Exclusion Criteria:

- any medication

- severe ilness

Study Design

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


Related Conditions & MeSH terms


Intervention

Other:
Hydrocortisone
Effects of hydrocortisone compared to placebo on cognition

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 test: Multifaceted Empaty test 25 min No
Secondary memory autobiographic memory test (AMT) 25 min No
Secondary cognitive flexibilty computer based test: task switch 10 min No
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