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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 belowSelect...
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 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 2 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 2 weeks
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.
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
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have a history of seizures.I have been diagnosed with fibromyalgia by a Carilion physician.You are not able to have an MRI for medical reasons.I cannot undergo CT scans due to health reasons.I have been diagnosed with CRPS type I or II by a Carilion doctor.
Research Study Groups:
This trial has the following groups:- Group 1: LIFU - CRPS
- Group 2: SHAM - CRPS
- Group 3: LIFU - FM
- Group 4: SHAM - FM
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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