- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00764088
A Retrospective Analysis of Patients With Full Thickness Wounds on a Case by Case Basis
November 24, 2015 updated by: Randall Wolcott, Southwest Regional Wound Care Center
To demonstrate the effectiveness or ineffectiveness of novel treating agents or agents used for compassionate rescue, subjects and their wounds will be analyzed retrospectively and their non-identifiable information will be compiled in the form of case studies.
Subjects who demonstrated characteristics of interest (e.g.
healing) as determined by the PI will be chosen for case studies.
Study Overview
Status
Completed
Conditions
Detailed Description
All wounds at the Southwest Regional Wound Care Center (WCC) are managed using anti-biofilm strategies.
When determining the therapeutic course for a patient and his full thickness wound, all management agents that are available are considered for use; and the clinician uses his judgment to determine the most appropriate tools to use that will give the patient the most likely chance of success.
Some of the agents that are used are novel, and it is appropriate to demonstrate to others the potential usefulness of these agents
Study Type
Observational
Enrollment (Actual)
4
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
Primary Care Clinic- Southwest Regional Wound Care Center
Description
Inclusion Criteria:
- Male or female > 18 years old
- Retrospective analysis
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 |
|---|
|
Anaysis of Full Thickness wounds
To demonstrate the effectiveness or ineffectiveness of novel treating agents or agents used for compassionate rescue, subjects and their wounds will be analyzed retrospectively and their non-identifiable information will be compiled in the form of case studies.
Subjects who demonstrated characteristics of interest (e.g.
healing) as determined by the PI will be chosen for case studies.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Retrospective Analysis of Patients with Full Thickness Wounds
Time Frame: 1 year
|
1 year
|
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 Major Dates
Study Start
August 1, 2007
Primary Completion (Actual)
June 1, 2008
Study Completion (Actual)
June 1, 2008
Study Registration Dates
First Submitted
September 29, 2008
First Submitted That Met QC Criteria
September 30, 2008
First Posted (Estimate)
October 1, 2008
Study Record Updates
Last Update Posted (Estimate)
November 26, 2015
Last Update Submitted That Met QC Criteria
November 24, 2015
Last Verified
November 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 56-RW-008
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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