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Hip Arthroscopy Versus Conservative Management of Femoroacetabular Impingement

U

University of Western Ontario, Canada

Status

Unknown

Conditions

Femoroacetabular Impingement

Treatments

Other: Physical therapy
Procedure: Arthroscopic hip surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT01621360
FKSMC-2011-01

Details and patient eligibility

About

The objective of this study is to determine if patients with femoroacetabular impingement (FAI) who undergo arthroscopic hip surgery experience similar outcomes at 2 years post-operative with respect to physical function, pain, and health related quality of life, compared to similar patients who receive conservative management, including medication and physiotherapy.

Full description

Arthroscopic surgery is now commonly used to treat patients with femoroacetabular impingement (FAI) however there is a lack of scientific evidence to support its efficacy. Two distinct types of FAI have been defined: cam impingement and pincer impingement. Cam impingement is described as an abnormally prominent anterolateral femoral head-neck junction that rubs against the acetabular rim during flexion resulting in impingement of the acetabular labrum. Pincer impingement is described as an anatomical overcoverage of the femoral head by the acetabulum that impinges the labrum leading to proliferation, or an increase in the prominence of the acetabular rim, further exacerbating the impingement. Previous studies investigating the efficacy of arthroscopic surgery of the knee and shoulder have shown no benefit compared to sham surgery and non-surgical management, therefore strong scientific evidence is needed to support its use in the treatment of hip pathology.

Enrollment

140 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with femoroacetabular impingement of the hip
  • 18 years of age or older
  • grade 1, 2 or 3 radiographic severity of osteoarthritis as defined by the Tonnis classification scale.

Exclusion criteria

  • identified isolated labral tear
  • inflammatory or post-infectious arthritis
  • previous arthroscopic treatment for hip osteoarthritis
  • previous major hip trauma
  • Tönnis grade 4 osteoarthritis in two compartments in persons over 60 years of age.
  • patients with a major neurologic deficit, serious medical illness (life expectancy less than 2 years or high intraoperative risk) or those who are unable to provide informed consent or who are deemed unlikely to comply with follow-up.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

140 participants in 2 patient groups

Arthroscopic surgery
Active Comparator group
Description:
Arthroscopic surgery of the hip plus optimized medical management
Treatment:
Procedure: Arthroscopic hip surgery
Conservative management
Active Comparator group
Description:
Physical therapy aimed at strengthening and stabilization of the hip and appropriate analgesic and anti-inflammatory medication.
Treatment:
Other: Physical therapy

Trial contacts and locations

1

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Central trial contact

Stacey Wanlin

Data sourced from clinicaltrials.gov

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