Greater Trochanteric Pain Syndrome

6

Review clinical trials related to Greater Trochanteric Pain Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

ReneuRx™ (Nerve Selective Therapy) Utilized in Lateral Hip Pain

The goal of this clinical trial is to evaluate the safety and analgesic performance of the ReneuRx™ device in subjects with moderate to severe chronic lateral hip pain compared to subjects receiving treatment with corticosteroid injection in adults aged 22-80 years. Participants will attend study visits and complete quality of life questionnaires. Participants will be followed for approximately 6-12 months after the study procedure.

Participants needed: 100
Trial details
Age: 22-80Biological sex: AllType: InterventionalSponsor: Brixton Biosciences, Inc.Updated: Jun 29, 2026Locations: 11
Eligibility criteria

Age 22 to 80, inclusive of any gender [+6]

Known allergy to glycerol, hyaluronic acid, poloxamer 407, or phosphate buffered... [+27]

Status: Recruiting

Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS)

The objective of this study is to evaluate how an ultrasound-guided percutaneous procedure, TENEX, can help people with chronic hip pain resulting from a condition called Greater Trochanteric Pain Syndrome (GTPS) and to characterize the efficacy of percutaneous tenotomy (PUT) using TENEX®, a device used for the treatment of various tendinopathies. In this study an ultrasound (US) is performed to guide the partial release of gluteus medius and minimus and Iliotibial band tendons in patients diagnosed with refractory Greater Trochanteric Pain Syndrome (GTPS) vs control. The investigator team hypothesizes that the new TENEX can improve the pain level for individuals with GTPS to help those individuals perform their activities of daily living (ADLs), e.g., walking, standing, and side-lying, as well as demonstrate less medication utilization. The study predicts that this percutaneous outpatient procedure can decrease pain, increase mobility, and decrease medication utilization. The study team hypothesizes that PUT can improve the pain level and function for individuals suffering with GTPS. The study will assess walking, standing, and side-lying tolerance, as well as medication utilization. The investigator team predicts that this percutaneous outpatient procedure can decrease pain and medication utilization while increasing mobility.

Participants needed: 150
Trial details
Age: 30-90Biological sex: AllType: InterventionalSponsor: Montefiore Medical CenterUpdated: May 8, 2026Locations: 1
Eligibility criteria

Aged 18-90 [+3]

Significant mobility restrictions; people using wheelchairs [+2]

Status: Not yet recruiting

Outcomes From Hyperbaric Oxygen (HBO2) Treatment for Emerging Indications

This study will evaluate the effectiveness of hyperbaric oxygen therapy (HBOT) on treating emerging indications (i.e., conditions that have shown to potentially benefit from HBOT) using the Multicenter Registry for Hyperbaric Oxygen Treatment. The study team aims to collect ongoing data on how well HBOT treats these emerging indications, and to add these data to the growing HBO Registry. The research team hypothesizes that HBOT will result in improvements of the condition of the various emerging indications.

Participants needed: 100
Trial details
Phase: Phase 4Biological sex: AllType: InterventionalSponsor: Jay C. Buckey Jr.Updated: May 5, 2026
Eligibility criteria

Patients referred for HBOT with an emerging indication

Contraindication to hyperbaric oxygen treatment (untreated seizures, pneumothora... [+1]

Status: Recruiting

ESWT vs Conventional Physical Therapy in Greater Trochanteric Pain Syndrome

This study aims to compare the effectiveness of Extracorporeal Shockwave Therapy (ESWT) with conventional physical therapy in patients with Greater Trochanteric Pain Syndrome (GTPS). GTPS is a common cause of lateral hip pain, often related to gluteal tendinopathy rather than trochanteric bursitis. Sixty patients will be randomly assigned to two groups: ESWT or conventional physical therapy (TENS, hot pack, ultrasound). Pain (VAS), hip function (Harris Hip Score), lower limb function (LEFS), and global improvement will be evaluated at baseline, week 3, and week 12. The purpose of this study is to determine which treatment provides greater pain relief and functional improvement.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Kanuni Sultan Suleyman Training and Research HospitalUpdated: Jan 27, 2026Locations: 1
Eligibility criteria

Age between 18 and 65 years [+2]

Hip deformities [+7]

Status: Recruiting

Exercise and Patient Education for Patients With Lateral Hip Pain

This prospective cohort trial will investigate a progressive exercise protocol and patient education for patients with hip abductor tendon pathology. The primary outcome is patient reported pain measured by the revised Copenhagen Hip And Groin Outcome Score (HAGOS), that will be conducted at baseline and at a 12 week follow-up.

Participants needed: 60
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Jeppe LangeUpdated: Jun 26, 2025Locations: 1
Eligibility criteria

Age 18-75 years [+3]

Corticosteroid injection in the affected hip joint within the last six weeks pri... [+4]

Status: Recruiting

Feasibility of a Home Exercise Program With the Addition of a Corticosteroid Injection in Patients With Lateral Hip Pain

We have developed an exercise protocol that we plan to evaluate in a future randomized controlled trial in combination with a corticosteroid injection. In accordance with the MRC Framework of Complex Interventions, which reccomends stepwise development of interventions and testing of feasibility before applying them to a trial, we aim to evaluate the feasibility of our intervention before initiating further trials. The purpose of this non-randomized feasibility study is to test the feasibility and acceptability of this exercise protocol with addition of a corticosteroid injection with no aim of evaluating effects. All participants in this study will receive the following interventions: * An ultrasound-guided corticosteroid injection superficial to the insertion of the gluteus medius and minimus tendons on the greater trochanter of the hip. * A home exercise program including 3 exercises, scalable to 3 different difficulty levels. * A patient information leaflet containing relevant information on managing lateral hip pain.

Participants needed: 20
Trial details
Age: 35+Biological sex: AllType: InterventionalSponsor: Aalborg UniversityUpdated: Jun 13, 2024Locations: 1
Eligibility criteria

35 years of age [+6]

Corticosteroid injection in the affected hip or other new treatment by a health... [+7]