Mechanisms Regulating Wound Vascularization

Sponsor
Gayle Gordillo (Other)
Overall Status
Terminated
CT.gov ID
NCT00737321
Collaborator
(none)
36
2
124
18
0.1

Study Details

Study Description

Brief Summary

This pilot study is designed to assess the impact of ischemia/ diminished wound vascularization and stress on wound healing by comparing patterns of gene expression in specific cell types critical to wound healing biology, e.g. macrophages or endothelial cells.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Samples will be collected

Detailed Description

Chronic wounds affect approximately 2% of the U.S. population at any given time. Animal models can not simulate the complex set of pre-existing conditions in each individual that results in failed wound healing. Therefore, human subjects must be used to obtain valid data. Adequate wound vascularization that permits blood vessels to deliver oxygen to the wound is a requirement for wound healing to occur. This protocol will attempt to gain greater understanding of the mechanisms of chronic wounds through 3 specific aims: 1) identify the angiogenic mechanisms in wound site macrophages, which are required for healing, 2) determine the impact of stress and glucocorticoid resistance on endothelial cell and macrophage biology and ultimately wound healing outcomes, 3) identify patterns of gene expression in wound endothelial cells that are found in healing versus non-healing wounds. This data will be correlated with the wound oxygenation status to determine the impact of wound vascularization on the observed biological responses.

Study Design

Study Type:
Observational
Actual Enrollment :
36 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Mechanisms Regulating Wound Vascularization
Actual Study Start Date :
Aug 1, 2008
Actual Primary Completion Date :
Dec 1, 2018
Actual Study Completion Date :
Dec 1, 2018

Arms and Interventions

Arm Intervention/Treatment
2- Diabetics without wound (s)

These group of subject will be control arm, included who have good glycemic control diabetic with HbA1c 8.4 or lower and also without any open wounds. Samples will be collected.

Procedure: Samples will be collected
wound tissue biopsy, blood samples, saliva collection and wound VAC sponge (if applicable).

1-Subjects with diabetes with wound

This group of subjects will have wound and come for couple of follow up visits for saliva collection, biopsy collection and blood draw.

Outcome Measures

Primary Outcome Measures

  1. Changes in Gene Expression Profile in Healing versus Non-healing Wounds [12 weeks]

    Wound tissue biopsies, saliva, serum samples and wound sponges will be obtained at an initial time point, at the midpoint of the study and near the end of wound closure over a 12 week window. If the wound closes quickly, i.e. less than 4 weeks then only 2 biopsies will be obtained.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 69 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18-69 years

  • ischemic wound group

  • non-ischemic wound group

  • diabetes with good glycemic control

  • lower extremity wound

Exclusion Criteria:
  • Age greater ≥ 70 years

  • End stage renal disease

  • Unable to provide informed consent

  • Pregnant women

  • Therapeutically anticoagulated

  • Prisoners

  • Periwound TcOM < 25mmHg

  • Spinal cord injury

  • Taking immunosuppressive medications

  • Individuals with current diagnosis of a major psychiatric illness (e.g.schizophrenia,psychosis)

  • Severe protein malnutrition- pre-albumin < 10 mg/dl or albumin < 2 g/dl

  • Diabetes with poor glucose control-defined as hgb A1c > 8.4%

Contacts and Locations

Locations

Site City State Country Postal Code
1 OSU East Wound Care Center Columbus Ohio United States 43205
2 OSU Comprehensive Wound Care Center Morehouse Columbus Ohio United States 43221

Sponsors and Collaborators

  • Gayle Gordillo

Investigators

  • Principal Investigator: Gayle Gordillo, MD, Ohio State University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gayle Gordillo, Professor, Ohio State University
ClinicalTrials.gov Identifier:
NCT00737321
Other Study ID Numbers:
  • 2008H0051
First Posted:
Aug 19, 2008
Last Update Posted:
Dec 1, 2021
Last Verified:
Nov 1, 2021
Keywords provided by Gayle Gordillo, Professor, Ohio State University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 1, 2021