- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00764348
Evaluation of Wound Biofilm in Acute and Chronic Wounds
September 6, 2011 updated by: Randall Wolcott, Southwest Regional Wound Care Center
Patients who present to a wound care center for management of their wounds will be evaluated clinically to establish if their wounds are chronic or acute.
These patients will undergo standard of care management of their wounds.
If debridement is indicated for the patient, the patient will be asked to participate in a study.
Once the standard of care debridement is complete, the material debrided from the wound, instead of being discarded into a biohazard bag, will be prepared for shipment.
The samples will then be shipped to the Center for Biofilm Engineering where microscopic evaluation will be conducted on the material.
Conclusion will be made from that analysis.
Study Overview
Detailed Description
A planktonic concept of the bacteria present on the surface of a chronic wound is no longer viable.
Microscopic studies show that biofilm is present on chronic wounds yet does not seem to be prominent on the surface of acute wounds.
Biofilm is able to neutralize our host defenses and commandeer host systems, and possesses an impressive array of defenses and virulence factors.
Clinically we see a significant difference in the healing behavior between chronic and acute wounds.
Also, suppression of biofilm using multiple simultaneous strategies including debridement, anti-biofilm agents, specific biocides, antibiotics and advanced technologies improves wound healing.
This suggests biofilm plays an important role in delayed wound healing.
Study Type
Observational
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Acute and Chronic Wounds
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
no treatment
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
It is important for all wound care providers to firmly grasp the wound biofilm concept, its importance in delayed wound healing, and how it differs from a planktonic bacterial concept.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
September 30, 2008
First Submitted That Met QC Criteria
October 1, 2008
First Posted (Estimate)
October 2, 2008
Study Record Updates
Last Update Posted (Estimate)
September 7, 2011
Last Update Submitted That Met QC Criteria
September 6, 2011
Last Verified
September 1, 2011
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 56-RW-002
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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