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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01169974
Other study ID # CHU P 2010-18
Secondary ID
Status Completed
Phase N/A
First received July 23, 2010
Last updated October 30, 2017
Start date February 1, 2011
Est. completion date December 4, 2012

Study information

Verified date October 2017
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators aim to test the hypothesis that Laser speckle contrast imaging allows for the measurement of cutaneous blood flow following various durations of tourniquet ischemia.


Description:

Ischemia and post occlusive reactive hyperemia in the skin is tested in healthy normal subjects for tourniquet ischemias of 1, 2 & 3 minutes at rest.


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date December 4, 2012
Est. primary completion date September 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Healthy volunteers

- Affiliation to the French health system

Exclusion Criteria:

- Any disease or chronic treatment

Study Design


Related Conditions & MeSH terms


Intervention

Other:
tourniquet ischemia
Recording of cutaneous blood flow on the forearm at rest before and following tourniquet ischemias of 1 , 2 & 3 minutes

Locations

Country Name City State
France University hospital Angers

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Laser speckle Peak value of laser speckle signal with 2 minutes of ischemia
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