NCT00764088

Brief Summary

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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
4

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Aug 2007

Shorter than P25 for all trials

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2007

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2008

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

September 29, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 1, 2008

Completed
Last Updated

November 26, 2015

Status Verified

November 1, 2015

Enrollment Period

10 months

First QC Date

September 29, 2008

Last Update Submit

November 24, 2015

Conditions

Full Thickness Wounds

Keywords

full Thickness wounds

Outcome Measures

Primary Outcomes (1)

  • Retrospective Analysis of Patients with Full Thickness Wounds

    1 year

Study Arms (1)

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.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Primary Care Clinic- Southwest Regional Wound Care Center

You may qualify if:

  • Male or female \> 18 years old
  • Retrospective analysis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Randall Wolcott, MD

    Southwest Regional Wound Care Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 29, 2008

First Posted

October 1, 2008

Study Start

August 1, 2007

Primary Completion

June 1, 2008

Study Completion

June 1, 2008

Last Updated

November 26, 2015

Record last verified: 2015-11