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.
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