Point-of-Care Ultrasound in Greater Trochanteric Pain Syndrome

NCT ID: NCT01642043

Last Updated: 2022-08-29

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 100 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2012-06-30
• Study Completion Date: 2015-08-31

Brief Summary

Greater trochanteric pain syndrome (GTPS) is a common cause of musculoskeletal pain.

The primary aim of this study is to describe the soft tissue and bony structural ultrasound (US) findings identified in the lateral hip and iliotibial band (ITB) in patients presenting with greater trochanteric pain syndrome (GTPS) in an outpatient rheumatology clinic.

Detailed Description

GTPS, widely known as trochanteric bursitis, encompasses a spectrum of disorders (gluteal tendinopathy, tears, bursitis, and ITB syndrome) that are difficult to distinguish by clinical exam alone. Better understanding of US imaging characteristics in relation to clinical symptoms may be helpful in identifying those patients who would most benefit from corticosteroid injections and other non-operative treatment options.

Point-of-care musculoskeletal US use has been shown to reduce repeated hospital appointments, improve accuracy of diagnosis, and provide expedited treatment, thus improving quality of care in an outpatient musculoskeletal clinic. US assessment is not routinely included in the management of GTPS patients and ideal imaging modalities are not established.

Conditions

Greater Trochanteric Pain Syndrome

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Lateral hip pain thought to be due to GTPS as evidenced by tenderness to palpation of the lateral hip over the greater trochanter
• Have a pain score of at least 2 out of 10 on an 11-point numeric rating scale
• Lateral hip pain for at least 1 week
• For participants with bilateral GTPS, the most symptomatic hip will be considered the study hip
• Have a telephone

Exclusion Criteria

• Inability to give informed consent
• BMI > 40
• Evidence of severe OA of the study hip by X-ray
• Avascular necrosis of the study hip
• Groin pain at rest or with log-rolling
• Hip internal rotation range of motion < 15 degrees
• Prior fracture involving the study hip or femur
• Prior hip surgery or prosthesis in the painful hip
• Paralysis or paresis of the lower extremity
• Wheelchair bound
• Open wound or skin lesions in the lateral hip

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Massachusetts General Hospital

OTHER

Sponsor Role: lead

Responsible Party

Minna Jean Kohler

Director, Musculoskeletal Ultrasound- Division of Rheumatology, Allergy, and Immunology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Minna J. Kohler, M.D.

Role: PRINCIPAL_INVESTIGATOR

Massachusetts General Hospital

Locations

Massachusetts General Hospital

Boston, Massachusetts, United States

Countries

United States

Other Identifiers

2012p001126

Identifier Type: -

Identifier Source: org_study_id