Ultrasound Treatment on Wound Healing Time (GE-MTEC)

General Electric (GE)

Status: Terminated

Conditions: 2nd Degree Burn of the Skin; Burn Wound

Treatments: Device: Pulsed splenic ultrasound; Device: Ultrasound probe (no energy applied)

Study type: Interventional

Funder types: Industry

Identifiers

NCT05796492

HS-22-00019

Details and patient eligibility

About

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).

Full description

The Central Hypothesis underlying this study is that splenic ultrasound stimulation activates the splenic anti-inflammatory pathway, thereby producing reduction in circulating macrophage cytokine production, reduction of neutrophil invasiveness, or induction of phenotypic transition in circulating immune cells (e.g., M1 to M2 transition in macrophages) in patients with partial thickness wounds that cover <20% body surface area.

Approximately 24 subjects will participate in this study. Male and female subjects of all races and ethnicities will be recruited for study from the ethnically diverse patient population of the LAC+USC Burn Center from the surrounding area.

Phase 0

Burn wound subjects will be screened and enrolled at the LAC+USC Burn Center located in Los Angeles, California. No other sites, neither regional nor outside of the United States are going to participate in enrollment of subjects.

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.

12 months.

28 days or until healed (whichever comes first)

Enrollment: 8 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Male or Female aged 18 or older
• Second-degree burn wounds of less than 20% total body surface area (TBSA)
• No active wound infection at screening based on clinical criteria
• Able to provide written informed consent

Exclusion criteria

• Wounds determined by study clinicians to be ineligible, including those that may inhibit access to the spleen for the ultrasound procedure

• Participating in another research study that may affect the conduct of results of this study

• BMI > 30

• Having or exhibiting any of the following:

  • Previous surgery of the spleen, esophagus, stomach, duodenum, or liver, including splenectomy
  • End stage renal disease and/or uremia
  • Active malignancy
  • Previous leukemia and/or lymphoma
  • Human immunodeficiency virus infection or AIDS
  • Rheumatoid arthritis or other immune-mediated diseases (e.g., inflammatory bowel disease
  • Arrythmias, including but not limited to, atrial fibrillation, atrial flutter, clinically significant bradycardia, ventricular arrhythmias, and A-V block
  • Implanted pacemaker or cardioverter/debribrillator
  • History of unstable angina, angioplasty or coronary arterial by-pass grafting surgery
  • History of stroke or TIA
  • Untreated thrombosis or bleeding disorders
  • Currently implanted vagus nerve stimulator
  • Currently implanted spinal cord stimulator or other chronically implanted electronic device

• Receiving oral, topical, rectal, or parenteral corticosteroids in an unstable dose 4 weeks prior to baseline visit

• Any immunosuppressive or cytotoxic medications

• Clinically relevant history of alcohol or drug abuse as determined by the investigator including:

  • alcohol consumption within 4 days of the baseline visit
  • tobacco or nicotine product use within the past 1 month
  • recreational drug use within the past 1 month

• Pregnant or breast feeding

• Unable or unwilling to comply with study procedures

• Have recently (within 3 months) been diagnosed with COVID, or have ever been diagnosed with long COVID

• Have an autoimmune disorder, such as, rheumatoid arthritis or lupus

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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8 participants in 2 patient groups

LOGIQ E10 Sham

Sham Comparator group

Description:

The sham condition will consist of the ultrasound probe placed over the spleen with no energy applied.

Treatment:

Device: Ultrasound probe (no energy applied)

LOGIQ E10 ultrasound Active

Active Comparator group

Description:

The intervention condition will receive 10 minutes of splenic ultrasound daily.

Treatment:

Device: Pulsed splenic ultrasound