Bacterial Load for Integra™ in Operative Wounds

Status unconfirmed

Conditions studied: Wounds and Injuries

In brief

Proportion of postoperative complications (infections, dehiscence, graft slough) after initial application of Integra™

Key facts

Study ID

NCT04543240

Run by

Georgetown University

People needed

54

Starts

2017-12-14

Expected to finish

2021-01-01

Last updated by the study team

2020-09-11

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or Female age 18-90.
• Full-thickness wounds below the knee.
• Patients who require, in the opinion of the Investigator, operative application of Integra™.
• Patients able and willing to comply with the study protocol.

You may not qualify if…

• Male or Female under 18 or over 90
• Patients that do not have Full-thickness wounds below the knee
• Patients who do not require, in the opinion of the Investigator, operative application of Integra™.
• Patients that are not able or willing to comply with the study protocol.

Where it is running

• MedStar Georgetown University Hospital — Washington D.C., District of Columbia, United States (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.