Actively Recruiting

Phase Not Applicable
Age: 40Years - 80Years
All Genders
ID05206838

Achilles Tendon Homograft for the Treatment of Gluteus Medius Insufficiency After Hip Replacement

Led by Sahlgrenska University Hospital · Updated on 2025-04-08

44

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

S

Sahlgrenska University Hospital

Lead Sponsor

G

Göteborg University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Residual limping due to gluteus medius insufficiency after total hip replacement is a serious complication without effective treatment. This study aims to compare surgical reconstruction of the gluteus medius using an Achilles tendon allograft with non-surgical physiotherapy treatment. The hypothesis is that surgery followed by physiotherapy will improve hip function and reduce limping more than physiotherapy alone. Participants are randomly assigned to one of two groups. One group undergoes surgical reconstruction where an Achilles tendon allograft with a calcaneus block is fixed to the greater trochanter and tensioned through the gluteus medius muscle, followed by partial weight bearing for 2 months and 10 months of physiotherapy. The other group receives only physiotherapy for 12 months without surgery. Throughout the study, participants will be assessed at 12 months using the Oxford Hip Score to measure hip function. Additional evaluations include Trendelenburg's sign, hip abduction strength, activity levels, quality of life indexes, and monitoring of any adverse events. The total study duration for each participant is 12 months, with close observation of treatment outcomes and safety.

CONDITIONS

Brief Title

Achilles Tendon for the Treatment of Gluteus Medius Insufficiency

Who Can Participate

Age: 40Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Persisting limping with positive Trendelenburg's sign for at least 12 months after total hip arthroplasty
  • Rupture or avulsion of the gluteus medius tendon verified with ultrasound or MRI
  • Leg length discrepancy less than 1 cm
  • Femoral offset discrepancy less than 25%
Not Eligible

You will not qualify if you...

  • Neuromuscular disorders

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - 2 months

Participants undergo surgical reconstruction of the gluteus medius using an Achilles tendon allograft fixed between the muscle and the greater trochanter, followed by immediate post-operative care including partial weight bearing.

Visits as needed during partial weight bearing period

Treatment

Duration - 10 to 12 months

Participants receive physiotherapy following surgery or physiotherapy alone if non-surgical, aimed at improving hip function and reducing limping.

Regular physiotherapy visits during this period

Trial Site Locations

Total: 1 location

1

Sahlgrenska University Hospital

Mölndal, Sweden, 431 80

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Incidence and treatment of abductor deficiency during total hip arthroplasty using the posterior approach: repair with direct suture technique and gluteus maximus flap transfer.

L A Whiteside, M E Roy

https://pubmed.ncbi.nlm.nih.gov/31146555

Post-operative gait analysis in total hip replacement patients-a review of current literature and meta-analysis.

Alistair M Ewen, Su Stewart, Alan St Clair Gibson...

https://pubmed.ncbi.nlm.nih.gov/22410129