Status:
COMPLETED
Obtaining and Storing Blood Samples and Debridement Samples for Wound Related Research
Lead Sponsor:
Southwest Regional Wound Care Center
Conditions:
Venous Insufficiency
Eligibility:
All Genders
18+ years
Brief Summary
The intent of this protocol is to obtain blood samples from subjects with or without a wound, so the blood can be used in wound-related scientific studies. It is also the intent of this protocol to sa...
Detailed Description
The samples will be studied in order to attempt to better understand wounds and their associated barriers to healing. Analytical methods used to examine the blood or debridement can investigate morpho...
Eligibility Criteria
Inclusion
- Inclusion Criteria for the Collection of Wound Debridement
- The subject must have a full thickness wound.
- The subject must be a candidate for sharp debridement.
- The subject must be 18 years of age or older.
- The subject must be mentally competent as determined by the Investigator Inclusion Criteria for the Collection of Blood
- Wounded or Otherwise Not Healthy Subjects, Subjects Weighing Less Than 110 lbs., or Subjects Contributing 50ml of Blood or Less:
- The subject must be 18 years of age or older.
- The subject must be mentally competent as determined by the Investigator.
- Not Wounded and Healthy Subjects Weighing at Least 110 lbs. Who May Contribute Up To 500ml of Blood:
- The subject must be 18 years of age or older.
- The subject must be mentally competent as determined by the Investigator.
- The subject must weigh at least 110 lbs.
- The subject must have a hemoglobin level that is in or above the normal range within the last 8 (eight) weeks as determined by standard clinical laboratory testing, the copper sulfate test, or a point of care instrument.
Exclusion
- Exclusion Criteria for the Collection of Wound Debridement and Blood Collection\*
- The subject must not be currently incarcerated or pregnant.
- The subject must not weigh less than 40 lbs.
- If the subject will be contributing more that 50 ml of blood during an 8 (eight) week period, then the subject must not have donated red blood cells within the last 8 (eight) weeks.
Key Trial Info
Start Date :
June 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 1 2012
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00762697
Start Date
June 1 2007
End Date
April 1 2012
Last Update
November 26 2015
Active Locations (1)
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1
Southwest Regional Wound Care Center
Lubbock, Texas, United States, 79410