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Clinical Trials/ISRCTN33399646
ISRCTN33399646
Terminated
未知

Does the addition of an exercise programme improve outcomes in Greater Trochanter Pain Syndrome compared to corticosteroid injection and advice? A pilot study

Royal Devon & Exeter NHS Foundation Trust0 sites48 target enrollmentJuly 25, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Greater trochanter pain syndrome
Sponsor
Royal Devon & Exeter NHS Foundation Trust
Enrollment
48
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 25, 2018
End Date
May 1, 2021
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Aged 35\-70 years
  • 2\. Unilateral or bilateral trochanteric pain for greater than 3 months
  • 3\. Pain on walking and climbing slopes or stairs and/or lying on the affected side
  • 4\. Absence of groin pain
  • 5\. Tenderness on palpation of the greater trochanter
  • 6\. At least one of the following tests provocative of lateral hip pain: Combined hip flexion, abduction and external rotation (FABER); Active derotation test; Combined hip flexion, adduction and external rotation; Modified Ober test; 30 second single leg stance; Active hip abduction at end range adduction in side lying
  • 7\. Hip osteoarthritis excluded radiologically

Exclusion Criteria

  • 1\. Evidence of osteoarthritis on X\-ray (over grade 1\)
  • 2\. Previous lower limb surgery affecting gait
  • 3\. Arthroplasty of the affected hip
  • 4\. Other neuromuscular or musculoskeletal conditions affecting gait or ability to exercise
  • 5\. Corticosteroid injections/physiotherapy/extracorporeal shock wave therapy (ECSWT) for GTPS in the last 3 months
  • 6\. Range of hip flexion \<90 degrees
  • 7\. Significant lumbar pathology/pain
  • 8\. Previous lumbar nerve root entrapment or spinal surgery
  • 9\. Unable or unwilling to comply with study protocol
  • 10\. Unable or unwilling to offer written consent to the study

Outcomes

Primary Outcomes

Not specified

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