← Back to Search

Ultrasound Therapy

LIFU for Chronic Pain

N/A
Recruiting
Led By Elizabeth Stringer, MD
Research Sponsored by Carilion Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Diagnosis of fibromyalgia (FM) by Carilion physician (American College of Radiology 2011 modified fibromyalgia criteria)
Diagnosis of complex regional pain syndrome (CRPS) I or II (Budapest Criteria) by Carilion physician
Must not have
History of seizures and/or pseudo-seizures
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 2 weeks

Summary

This trial is testing a new therapy called low-intensity focused ultrasound (LIFU) for people with chronic pain conditions like CRPS and FM. LIFU uses gentle sound waves to target specific brain areas to help reduce pain. The study aims to see if this therapy can lower pain levels and improve other symptoms in these patients.

Who is the study for?
This trial is for individuals with chronic pain conditions, specifically diagnosed with fibromyalgia or complex regional pain syndrome by a Carilion physician. Participants must meet certain diagnostic criteria and cannot have contraindications to MRI or CT scans, nor a history of seizures.
What is being tested?
The study is testing the effectiveness of Low-intensity Focused Ultrasound (LIFU) as a neuromodulation treatment for chronic pain. Some participants will receive real LIFU while others will get a sham procedure to compare outcomes.
What are the potential side effects?
Since this trial involves non-invasive ultrasound technology, side effects are expected to be minimal but may include discomfort at the site of application or temporary changes in sensation.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have been diagnosed with fibromyalgia by a Carilion physician.
Select...
I have been diagnosed with CRPS type I or II by a Carilion doctor.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
Select...
I have a history of seizures.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 2 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 2 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Perceived Pain scores
Secondary study objectives
Clinical outcome - skin temperature
Clinical outcomes - circumference

Trial Design

4Treatment groups
Active Control
Placebo Group
Group I: LIFU - CRPSActive Control1 Intervention
Real LIFU application for CRPS cohort.
Group II: LIFU - FMActive Control1 Intervention
Real LIFU application for FM cohort.
Group III: SHAM - CRPSPlacebo Group1 Intervention
Sham LIFU application for CRPS cohort.
Group IV: SHAM - FMPlacebo Group1 Intervention
Sham LIFU application for FM cohort.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for fibromyalgia, such as Low-Intensity Focused Ultrasound (LIFU), Transcutaneous Electrical Nerve Stimulation (TENS), Scrambler therapy, and acupuncture, primarily work through neuromodulation. These techniques aim to alter neural activity to reduce pain perception and improve other symptoms like fatigue and mood disturbances. For instance, LIFU targets specific brain regions to modulate pain pathways, while TENS and Scrambler therapy use electrical currents to interfere with pain signals. Acupuncture may stimulate nerve endings to release pain-relieving chemicals. Understanding these mechanisms is important for fibromyalgia patients as it provides insight into how these treatments can potentially alleviate their symptoms and improve their quality of life.
Alteration of cortical excitability in patients with fibromyalgia.

Find a Location

Who is running the clinical trial?

Carilion ClinicLead Sponsor
80 Previous Clinical Trials
15,203 Total Patients Enrolled
Virginia Polytechnic Institute and State UniversityOTHER
153 Previous Clinical Trials
25,056 Total Patients Enrolled
Elizabeth Stringer, MDPrincipal InvestigatorCarilion Clinic
1 Previous Clinical Trials
80 Total Patients Enrolled

Media Library

Low-intensity Focused Ultrasound (LIFU) (Ultrasound Therapy) Clinical Trial Eligibility Overview. Trial Name: NCT05751096 — N/A
Musculoskeletal Disease Research Study Groups: LIFU - CRPS, SHAM - CRPS, LIFU - FM, SHAM - FM
Musculoskeletal Disease Clinical Trial 2023: Low-intensity Focused Ultrasound (LIFU) Highlights & Side Effects. Trial Name: NCT05751096 — N/A
Low-intensity Focused Ultrasound (LIFU) (Ultrasound Therapy) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05751096 — N/A
~2 spots leftby Jan 2025