Actively Recruiting

Age: 21Years - 80Years
All Genders
ID00777712

Mechanisms Underlying Impaired Wound Healing

Led by University of Pittsburgh · Updated on 2026-06-05

250

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research focuses on understanding the impaired wound healing process in people with diabetes by studying inflammatory cells from chronic wounds. It compares these wound-derived cells with normal blood-derived cells to explore the mechanisms behind dysregulated inflammation in diabetic individuals. The study aims to uncover molecular reasons for poor wound healing in diabetes to improve future treatments. Participants include adults aged 21 to 80 with chronic wounds lasting more than four weeks, including both diabetic and non-diabetic individuals. The study involves collecting blood samples and wound material using a VAC sponge, which is normally discarded during standard care. No treatments are given as this is an observational study. During the study, researchers will assess wound healing progress at 16 weeks and check infection status at the start. Participants' wound and blood cells will be analyzed to compare inflammation and healing mechanisms. The total duration of participation varies, focusing on biological sample collection and monitoring wound healing over time.

CONDITIONS

Brief Title

Mechanisms Underlying Impaired Diabetic Wound Healing

Who Can Participate

Age: 21Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 21-80
  • Presence of a chronic wound lasting more than 4 weeks
  • Both diabetic and non-diabetic individuals
  • Adult surgical wounds
Not Eligible

You will not qualify if you...

  • Unable to provide consent
  • Pregnant women
  • Therapeutically immunocompromised individuals
  • Individuals considered vulnerable under federal regulations (45 CFR 46 Subparts B, C, and D) or other vulnerable populations

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

Duration - Single day

Participants provide blood samples and wound fluid for analysis of wound healing mechanisms.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 16 weeks

Participants’ wound healing progress is observed over time without active intervention.

Periodic visits up to Week 16

Trial Site Locations

Total: 2 locations

1

UPMC Montefiore

Pittsburgh, Pennsylvania, United States, 15219

Actively Recruiting

2

UPMC Presbyterian

Pittsburgh, Pennsylvania, United States, 15219

Actively Recruiting

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Research Team

P

Piya Das Ghatak, PhD, MS

U

Urmila Gnyawali

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial