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Not Yet Recruiting NCT05710627

Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS)

Conditions: Greater Trochanteric Pain Syndrome

Sex: All
Ages: 18 Years – 90 Years
Phase: NA
Enrollment: 117
Sponsor: Montefiore Medical Center

Location: United States

Summary

The aim of this study is 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 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.

Eligibility Criteria

Inclusion Criteria:Aged 18-90People with GTPS of all different levels and etiologies confirmed with MRI or CT scanAbility to give informed consent forms independentlyFailed conservative medical treatment for at least 6 monthsExclusion Criteria:Significant mobility restrictions; people using wheelchairsPrevious surgery to the GMed or ITB

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05710627). StuddyBuddy aggregates publicly available trial information.