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A Study of the Effects of Molecular Diagnostic Directed Wound Gels on Wound Care Outcomes

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01319149
Recruitment Status : Completed
First Posted : March 21, 2011
Last Update Posted : September 13, 2012
Sponsor:
Information provided by (Responsible Party):
Randall Wolcott, Southwest Regional Wound Care Center

Brief Summary:
A retrospective molecular diagnostic review on wound care outcomes. The time periods include March, April, May of 2010.The retrospective review would analyze the days of healing during the timeframe, upon the introduction of molecular diagnostic testing

Condition or disease
Wounds

Detailed Description:
The null hypothesis would be that the introduction of molecular methods did not statistically affect patient outcomes. To study this hypothesis, our chief information technologist would query the database for any patients who are admitted during that time period. This period of time designated is March, April and May 2010.

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Study Type : Observational
Actual Enrollment : 400 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: A Retrospective Study Of the Effects of Molecular Diagnostic Directed Wound Gels on Wound Care Outcomes
Study Start Date : November 2010
Actual Primary Completion Date : September 2011
Actual Study Completion Date : September 2011

Resource links provided by the National Library of Medicine


Group/Cohort
No treatment
Patient records would be extracted from the electronic health record system of Southwest Regional Wound Care Center and placed in a separate bin.



Primary Outcome Measures :
  1. The retrospective review would analyze the days of healing during the timeframe, upon the introduction of molecular diagnostic testing. [ Time Frame: 1 yr ]
    To study this hypothesis, our chief information technologist would query the database for any patients who are admitted during that time period. This period of time designated is March, April and May 2010.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with wounds who have been treated at Southwest Regional Wound Care Center.
Criteria

Inclusion Criteria:

  • Patients who have been treated at SWRWCC during the months of March, April, or May 2010.

Exclusion Criteria:

  • Patients who were not treated at SWRWCC during the time frame of March, April or May 2010.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01319149


Locations
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United States, Texas
Southwest Regional Wound Care Center
Lubbock, Texas, United States, 79410
Sponsors and Collaborators
Southwest Regional Wound Care Center
Investigators
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Principal Investigator: Randall D Wolcott, M.D. Southwest Regional Wound Care Center
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Responsible Party: Randall Wolcott, Principal Investigator, Southwest Regional Wound Care Center
ClinicalTrials.gov Identifier: NCT01319149    
Other Study ID Numbers: 56-RW-020
First Posted: March 21, 2011    Key Record Dates
Last Update Posted: September 13, 2012
Last Verified: September 2012
Keywords provided by Randall Wolcott, Southwest Regional Wound Care Center:
molecular methods
Additional relevant MeSH terms:
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Wounds and Injuries