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
• Status: Enrolling by invitation
• 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
• 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.

Related Conditions & MeSH terms

• Wound
• Wounds and Injuries

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