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NCT00759499 Clinical Trial

Obtaining and Storing Wound Debridment Samples For Immediate or Future Wound-Related Scientific Study

Wound Clinical Trial

Official title:
Obtaining and Storing Wound Debridment Samples for Immediate or Future Wound-Related Scientific Study

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT00759499
Other study ID # 56-RW-004
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date January 2007
Est. completion date January 18, 2021

Study information
Verified date July 2020
Source Southwest Regional Wound Care Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Debridement Samples being collected for future or immediate research purposes.

Description:

Inclusion Criteria

1. The subject must have a full thickness wound.

2. The subject must be a candidate for sharp debridement.

3. The subject must be 18 years of age or older

4. The subject must be mentally competent as determined by the Principal Investigator.

Exclusion Criteria

1. The subject may not be currently incarcerated or pregnant.

- Nursing home and hospitalized subjects will not be excluded from this study because these subjects represent a large part of the wounded population.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 829
Est. completion date January 18, 2021
Est. primary completion date January 18, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 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 Principal Investigator

Exclusion Criteria:

- The subject may not be currently incarcerated or pregnant.

- Nursing home and hospitalized subjects will not be excluded from this study because these subjects represent a large part of the wounded population.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Soutwest Regional Wound Care Center Lubbock Texas

Sponsors (1)
Lead Sponsor Collaborator
Southwest Regional Wound Care Center

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary The intent of this protocol is to salvage wound material that is normally destined for destruction, so it can be used in wound-related scientific studies. 2 years
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