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NO Sensor to Record Wound Data in Acute or Chronic Wounds

NCT06944899 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-10-30

No results posted yet for this study

Summary

The purpose of this research is to evaluate the ability of a Nitric Oxide (NO) Sensor to collect NO measurement data from an open wound. Previous research suggests that NO levels may indicate the stage of healing the wound is in. This study is being done to determine if the NO Sensor can measure how much NO is in a participant's wound. The researcher will place the NO Sensor into a participant's wound to collect NO measurements for 30-60 minutes. The participant will then have 2 follow-up appointments to see how the wound heals over time.

Conditions

  • Volumetric Muscle Loss

Interventions

DEVICE

NO Sensor

NO sensor measuring wound characteristic data in wound bed

Sponsors & Collaborators

  • Defense Advanced Research Projects Agency

    collaborator FED

  • Stephen Badylak

    lead OTHER

Principal Investigators

  • Stephen Badylak, MD,DVM,PhD · University of Pittsburgh

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-05-20
Primary Completion
2025-10-28
Completion
2025-10-28

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06944899 on ClinicalTrials.gov