Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS)

Recruiting N/A Interventional Study
Greater Trochanteric Pain Syndrome
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
30 – 90
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Montefiore Medical Center · Other
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About This Trial
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 g…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Aged 18-90 * People with GTPS of all different levels and etiologies confirmed with MRI or CT scan * Ability to give informed consent forms independently * Failed conservative medical treatment for at least 6 months Exclusion Criteria: * Significant mobility restrictions; pe…
Contacts

Tahereh Naeimi, MD

3479778678

tnaeimi@montefiore.org

CONTACT