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Measurement of Blood Perfusion in Response to Loading in Patients With Wounds

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ClinicalTrials.gov Identifier: NCT02082041
Recruitment Status : Completed
First Posted : March 10, 2014
Last Update Posted : September 14, 2016
Sponsor:
Information provided by (Responsible Party):
Tamara Reid Bush, Michigan State University

Brief Summary:
The purpose of this study is to monitor the skin blood flow in the lower leg, with different levels and types of applied loads. These loads will not be placed over the patient's wound nor will they be higher than loads the skin normally experiences in daily activities. The results of this research will help investigators understand the development of pressure ulcers, commonly known as bedsores and stasis ulcers.

Condition or disease
Wound Formation

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Study Type : Observational
Actual Enrollment : 41 participants
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Study Start Date : June 2013
Actual Primary Completion Date : March 2016
Actual Study Completion Date : March 2016

Resource links provided by the National Library of Medicine


Group/Cohort
Wounds on leg



Primary Outcome Measures :
  1. Changes in perfusion [ Time Frame: Cross-sectional, evaluation time frame is approximately 2 hours occuring at the time of enrollment ]
    Skin perfusion will be measured as different loads are applied to the leg.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 100 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with wounds on their legs, wound clinic patients
Criteria

Inclusion Criteria:

  • Patients are eligible if he/she has a wound on one or both legs.

Exclusion Criteria:

  • under the age of 18
  • individuals with mental illness
  • individuals who are unable to sit for an hour
  • individuals whose wound care method prohibits testing

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): NCT02082041


Locations
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United States, Michigan
Sparrow Wound Clinic
Lansing, Michigan, United States, 48824
Sponsors and Collaborators
Michigan State University
Investigators
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Principal Investigator: Tamara Bush, PhD Michigan State University
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Responsible Party: Tamara Reid Bush, Principal Investigator, Michigan State University
ClinicalTrials.gov Identifier: NCT02082041    
Other Study ID Numbers: WOUND-MSU
First Posted: March 10, 2014    Key Record Dates
Last Update Posted: September 14, 2016
Last Verified: September 2016
Additional relevant MeSH terms:
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Wounds and Injuries