Magnetic Resonance Elastography of Myofascial Pain Syndrome

Overview

About this study

The purpose of this study is to develop MRE-based imaging biomarkers to measur the mechanical properties of the myofascial interface and determine if there are changes in these parameters in MPS patients and if these parameters can be used to monitor treatment responses and predict patient outcomes.

 

 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Healthy Volunteer Inclusion Criteria:

- Absence of a history of chronic pain in the targeted anatomical location (i.e., lower back and low extremities) that had limited activities of daily living or work.

- A numerical current pain index of less than 0.5 (on a 10-point Visual Analog Scale).

- Able to understand the goal of the project and give informed consent..

Healthy Volunteer Exclusion Criteria:

- Pregnancy or breastfeeding.

- Any contraindication to an MRI exam.

- Previous severe/acute back or low extremity injury (including fracture).

- Previous back or low extremity surgery.

- Back and lower limb deformities.

- Inability to provide consent.

Myofascial-Related Pain Patient Inclusion Criteria:

- A history of chronic low back or leg pain (the targeted location will be determined based on the findings in Aim 1) for at least 3 months. (Measured by patient history and physical exam).

- A palpable taut band or nodule within the skeletal muscle.

- Hypersensitive tender spot within the taut band.

- Recognition of current pain complaint by pressure on the tender nodule/taut band.

- Painful limit to the full stretch range of motion.

Myofascial-Related Pain Patient Exclusion Criteria:

- Pregnancy or breastfeeding.

- Any contraindication to an MRI exam.

- Previous therapy in the area to be treated within 6 months.

- Previous severe back or low extremity injury (including fracture) or surgery.

- Any neurological conditions or active systemic disease (e.g., diabetes, peripheral vascular disease, cancer, rheumatoid arthritis) that impaired sensation/pain perception.

- Severe osteoarthritis.

- Skin injuries in the area to be treated.

- Inability to provide consent.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Ziying Yin, Ph.D.

Open for enrollment

Contact information:

Timothy Waters M.S.

(507) 293-0692

Waters.Timothy@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20544033

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