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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02485405
Other study ID # SP15_CarolineLinninge
Secondary ID
Status Completed
Phase N/A
First received June 23, 2015
Last updated September 6, 2017
Start date June 2015
Est. completion date September 2017

Study information

Verified date September 2017
Source Lund University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to analyse gut permeability and stress.


Description:

Healthy male volunteers (aged 19-35 years) participate in Trier social stress test while saliva and blood samples are withdrawn.

Saliva will be used for analysis of cortisol and blood will be used for analysis of various biomarkers.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date September 2017
Est. primary completion date September 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 19 Years to 35 Years
Eligibility Inclusion Criteria:

- Man, 19-35 years old

- Healthy

Exclusion Criteria:

- Psychological disorders

- Use of antibiotics or other drugs

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Trier social stress test
Volunteers perform Trier social stress test

Locations

Country Name City State
Sweden Lund University Lund

Sponsors (1)

Lead Sponsor Collaborator
Lund University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary gut permeability (marker measured in plasma/serum) in healthy young men participating in Trier social stress test Volunteers will be followed by one hour after Trier social stress test
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