ClinicalTrials.Veeva

Menu

Evaluation of Non-Surgical and Arthroscopic Treatment for Hip Microinstability

G

Göteborg University

Status

Enrolling

Conditions

Hip Injuries
Musculoskeletal Abnormalities

Treatments

Procedure: physiotherapy
Procedure: arthroscopy

Study type

Interventional

Funder types

Other

Identifiers

NCT04934462
Hip Microinstability Study

Details and patient eligibility

About

Microinstability of the hip joint is an important cause of hip pain and reduced hip function in young and active individuals. Hip microinstability is due to extraphysiologic hip motion and could be secondary to acetabular dysplasia, connective tissue disorder, macrotrauma, microtrauma, iatrogenic- and idiopathic causes. Treatment for hip microinstability is initiated with non-surgical treatment consisting of physiotherapy aimed mainly at stability. If non-surgical treatment fails, surgery with arthroscopic plication of the hip joint capsule is the preferred method. This study evaluates non-surgical and arthroscopic treatment for hip microinstability regarding hip function and adverse events.

Full description

This is a prospective cohort study evaluating 26 participants above 18 years of age undergoing non-surgical and surgical treatment for microinstability of the hip joint. Participants with findings on physical examination and imaging suggestive of hip microinstability will undergo six months of physiotherapy aimed at stabilizing the hip joint. If non-surgical treatment fails, a diagnostic hip arthroscopy will be performed, and if hip microinstability is confirmed, the participants will undergo a plication of the hip joint capsule. Participants will be evaluated with Patient-Reported Outcome Scores (PROMs) and strength- and function tests at time of enrollment and at 6-, 12- and 24 months following treatment. The primary outcome is hip function determined by PROMs and strength- and function tests. Secondary outcomes include Health-Related Quality of Life (HRQL), sport activity level and adverse events.

Enrollment

26 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hip microinstability
  • Minimum 18 years old

Exclusion criteria

  • Hip osteoarthritis
  • Severe hip dysplasia
  • Perthes disease or avascular necrosis of the femoral head
  • Previous surgery to the hip joint

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

26 participants in 2 patient groups

non-surgical treatment
Other group
Description:
All participants will undergo 6 months of non-surgical treatment.
Treatment:
Procedure: physiotherapy
arthroscopic treatment
Other group
Description:
Those participants with failed non-surgical treatment at 6 months will undergo arthroscopic treatment.
Treatment:
Procedure: arthroscopy
Procedure: physiotherapy

Trial contacts and locations

3

Loading...

Central trial contact

Mikael Sansone, MD, PhD; Axel Öhlin, MD, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems