We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Methodological Issues and Laser Speckle Contrast Imaging (METHODO-LSCI)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01664572
First Posted: August 14, 2012
Last Update Posted: June 14, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
University Hospital, Angers
  Purpose
Microcirculation, especially skin microcirculation, is a window towards systemic vascular function in magnitude and underlying mechanisms. Different techniques have been developed to assess the microcirculation. Among these techniques, laser technology is used to perform non-invasive microvascular assessments. Although this technique is widely used, different methodological issues remain. This study aims at defining the way to use lasers for clinical use.

Condition
Microvascular Function

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Methodological Issues of Laser Speckle Contrast Imaging for Studying Microcirculation.

Further study details as provided by University Hospital, Angers:

Enrollment: 75
Study Start Date: June 2012
Study Completion Date: March 2016
Primary Completion Date: September 2015 (Final data collection date for primary outcome measure)
Groups/Cohorts
Healthy subjects

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Residents of France
Criteria

Inclusion Criteria:

  • age > 18years old
  • subject without any known cardiovascular disease

Exclusion Criteria:

  • pregnancy
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01664572


Locations
France
University Hospital
Angers cedex 9, France, 49933
Sponsors and Collaborators
University Hospital, Angers