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Ultrasound Treatment on Wound Healing Time

NCT05796492 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2025-01-17

No results posted yet for this study

Summary

This is a randomized, sham-controlled pilot study that will assess the safety and feasibility of splenic focused pulsed ultrasound treatment on burn wound healing time in 24 subjects (12 active ultrasound and 12 sham controls).

Conditions

  • Burn Wound
  • 2nd Degree Burn of the Skin

Interventions

DEVICE

Pulsed splenic ultrasound

A General Electric LOGIQ E10 ultrasound machine with a C1-6-XD clear probe, will be used to selectively deliver pulsed ultrasound to the spleen.

DEVICE

Ultrasound probe (no energy applied)

A General Electric LOGIQ E10 ultrasound probe will be placed over the spleen with no energy applied

Sponsors & Collaborators

  • General Electric Research

    lead INDUSTRY

Principal Investigators

  • David Armstrong, DPM, MD, PhD · USC Limb Preservation Consortium

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-22
Primary Completion
2024-12-18
Completion
2024-12-19
FDA Device
Yes

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 NCT05796492 on ClinicalTrials.gov