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Study identifier: NCT05710627 Synced from ClinicalTrials.gov · July 29, 2026
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Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS)

Condition: Greater Trochanteric Pain Syndrome  ·  Sponsor: Montefiore Medical Center

PhaseNA
Planned participants150
Who can joinAll sexes, 30 Years to 90 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Tahereh Naeimi, MD  ·  3479778678  ·  tnaeimi@montefiore.org

Always discuss trial participation with your own doctor first.

Locations (1)

Montefiore Medical CenterThe Bronx, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05710627