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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00759499
Enrollment
829
Registered
2008-09-25
Start date
2007-01-31
Completion date
2021-01-18
Last updated
2020-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wound

Keywords

study of debridement tissue for research purposes., open wound

Brief summary

Debridement Samples being collected for future or immediate research purposes.

Detailed 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.

Interventions

None listed

Sponsors

Southwest Regional Wound Care Center
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
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

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026