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Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS) (RCT GTPS)

Primary Purpose

Greater Trochanteric Pain Syndrome

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
TENEX
Sponsored by
Montefiore Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Greater Trochanteric Pain Syndrome

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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; people using wheelchairs Previous surgery to the GMed or ITB

Sites / Locations

  • Montefiore Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Treatment

Arm Description

Standard of care

TENEX device will be used

Outcomes

Primary Outcome Measures

Pain Level
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Pain Level
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Pain Level
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Pain Level
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Pain Level
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.

Secondary Outcome Measures

EQ-5D-5L
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
EQ-5D-5L
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
EQ-5D-5L
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
EQ-5D-5L
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
EQ-5D-5L
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.

Full Information

First Posted
January 24, 2023
Last Updated
September 18, 2023
Sponsor
Montefiore Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT05710627
Brief Title
Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS)
Acronym
RCT GTPS
Official Title
Evaluation of Percutaneous Tenotomy of the Gluteus Medius and Iliotibial Band for Greater Trochanteric Pain Syndrome (GTPS): A Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
December 2023 (Anticipated)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Montefiore Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed Description
Greater trochanteric pain syndrome (GTPS) is one of the most common causes of lateral hip pain in adults. GTPS is repetitive overload tendinopathy of the gluteus medius (GMed) and Iliotibial band (ITB), which play a primary role in hip abduction and pelvic stabilization in walking, stair climbing, running and standing on one leg. It is thought that the core pathology is greater trochanteric bursitis (TB) with or without coexisting gluteal tendinopathy. Some common etiologies include prolonged excessive pressure to the area, injury to the side of the hip, and repetitive movements; however, local steroid injections to the greater TB are not often successful over the long-term. The best estimates of prevalence are from a large, community-based study with over 3000 adults aged 50 to 70 years, in which unilateral GTPS was present in 15 percent of women and 6.6 percent of men. Patients who have not improved after at least 12 months of conservative medical management (CMM), including physical therapy, oral medications, or a local steroid injection have no other conservative treatment recourse. Open surgery for GMed or ITB tears is not recommended unless a tear is diagnosed on MRI. Based on a published study, a 60% improvement was shown in pain with the performance of TENEX of the GMed. The purpose of this project is to study the outcome of GMed and ITB PUT on CMM refractory GTPS. We want to quantify and show the scales of the pain in pre-operative and post-treatment cases. We also want to see how effective the surgery is in specific terms of pain levels because GTPS is a pain syndrome and reduction in pain level is the most important clinical factor. Patient Reported Outcome Measure (PROM) is one of the main outcomes that medical research is validated with and through this study we want to show the most important outcome of GTPS i.e., pain level (PROM for GTPS). Previous studies which focused on surgical outcomes have been mostly single-center trials. Pain and mobility impact patients' Quality of Life (QoL) and medical cost burden due to unemployment, psychosocial well-being, and functional dependence. The standard of care offered to address the pain and mobility needs of those with GTPS is to provide CMM, followed by open or arthroscopic surgery if surgery is indicated. However, there is a treatment gap for those patients who have failed CMM and are not surgical candidates. The authors submit that TENEX of the GMed and ITB may address this gap. The results from this research may have broad impacts on the treatment algorithm for patients with GTPS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Greater Trochanteric Pain Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
117 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard of care
Arm Title
Treatment
Arm Type
Experimental
Arm Description
TENEX device will be used
Intervention Type
Device
Intervention Name(s)
TENEX
Intervention Description
Use of TENEX device for sectioning of the gluteus medius and ITB tendons.
Primary Outcome Measure Information:
Title
Pain Level
Description
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Time Frame
Baseline (before the procedure)
Title
Pain Level
Description
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Time Frame
1-month
Title
Pain Level
Description
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Time Frame
3-month
Title
Pain Level
Description
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Time Frame
6-month
Title
Pain Level
Description
The difference in pain levels in patients before and after the procedure. Pain levels (NRS scale) recorded in the pre-operative visit will be compared to the pain levels at FU visits. Numeric rating scale(NRS) is a pain screening tool used to assess pain severity using a 0-10 scale, with 0 meaning no pain and 10 meaning the worst pain imaginable.
Time Frame
12-month
Secondary Outcome Measure Information:
Title
EQ-5D-5L
Description
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
Time Frame
Baseline (before the procedure)
Title
EQ-5D-5L
Description
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
Time Frame
1-month
Title
EQ-5D-5L
Description
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
Time Frame
3-month
Title
EQ-5D-5L
Description
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
Time Frame
6-month
Title
EQ-5D-5L
Description
In this study, we will also explore a comparative analysis between TENEX to conventional medical treatments. The study team will compare quality of life using the EQ-5D-5L. Walking, side-lying, sit-to-stand transfers, and medication utilization will be assessed as well. EQ-5D-5L is the descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1- digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a five digit number that describes the patient's health state.
Time Frame
12-month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
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; people using wheelchairs Previous surgery to the GMed or ITB
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tahereh Naeimi, MD
Phone
3479778678
Email
tnaeimi@montefiore.org
First Name & Middle Initial & Last Name or Official Title & Degree
Asude N. Hasanoglu, MD
Phone
9293778185
Email
ahasanoglu@montefiore.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sayed E. Wahezi, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Asude N. Hasanoglu, MD
Phone
929-377-8185
Email
ahasanoglu@montefiore.org
First Name & Middle Initial & Last Name & Degree
Tahereh Naeimi, MD
Phone
3479778678
Email
tnaeimi@montefiore.org
First Name & Middle Initial & Last Name & Degree
Sayed E. Wahezi, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
17678660
Citation
Segal NA, Felson DT, Torner JC, Zhu Y, Curtis JR, Niu J, Nevitt MC; Multicenter Osteoarthritis Study Group. Greater trochanteric pain syndrome: epidemiology and associated factors. Arch Phys Med Rehabil. 2007 Aug;88(8):988-92. doi: 10.1016/j.apmr.2007.04.014.
Results Reference
result
PubMed Identifier
32232066
Citation
Baker CL Jr, Mahoney JR. Ultrasound-Guided Percutaneous Tenotomy for Gluteal Tendinopathy. Orthop J Sports Med. 2020 Mar 19;8(3):2325967120907868. doi: 10.1177/2325967120907868. eCollection 2020 Mar.
Results Reference
result
PubMed Identifier
21893483
Citation
Del Buono A, Papalia R, Khanduja V, Denaro V, Maffulli N. Management of the greater trochanteric pain syndrome: a systematic review. Br Med Bull. 2012 Jun;102:115-31. doi: 10.1093/bmb/ldr038. Epub 2011 Sep 4.
Results Reference
result
PubMed Identifier
27139495
Citation
Mellor R, Grimaldi A, Wajswelner H, Hodges P, Abbott JH, Bennell K, Vicenzino B. Exercise and load modification versus corticosteroid injection versus 'wait and see' for persistent gluteus medius/minimus tendinopathy (the LEAP trial): a protocol for a randomised clinical trial. BMC Musculoskelet Disord. 2016 Apr 30;17:196. doi: 10.1186/s12891-016-1043-6.
Results Reference
result

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Evaluation of TENEX for Greater Trochanteric Pain Syndrome (GTPS)

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