Skip to content

Weightbearing Restrictions on Postoperative Outcomes Following Arthroscopic Surgery for FAI

Femoro Acetabular Impingement

The purpose of this single-blinded (assessor) randomized trial is to compare patient-reported, clinical and functional outcomes in patients randomized to weight-bearing as tolerated (WBAT) or partial weight-bearing (PWB) restrictions following arthroscopic surgery for femoroacetabular impingement (FAI) up to 12-months postoperative.

null

Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    16 to 50

Participation Criteria

Inclusion Criteria:

* 16 - 50 years of age at time of surgery
* Diagnosis of FAI (cam, pincer, mixed) based on the 2016 Warwick Agreement. All 3 criteria below must be met:

1. Symptoms of motion- or position-related pain in the hip or groin
2. Clinical signs consistent with FAI such as: decreased hip flexion and internal rotation, or positive impingement sign
3. Radiographic evidence (on BOTH x-ray AND non-contrast MRI) of intra-articular pathology consistent with FAI as determined by the treating surgeon.
* Failed conservative interventions of at least 3 months (i.e. physiotherapy)
* Have symptom relief with intra-articular injection of local anaesthetic
* Unilateral or bilateral surgical intervention (note: unilateral required to ensure the weight bearing guidelines are followed)
* Are willing to be followed for 12 months post-operative.

Eligibility for 'return to sport' cohort:

Additional assessment measures related to return to sport will be collected on the patient who meet the following criteria:

* are or were previously actively involved in sport as indicated by a pre-operative Hip Sports Activity Scale score of four of greater
* indicate a post-operative goal to return to sport following their procedure

Exclusion Criteria:

Clinical:

* Previous surgery on the affected hip, or other major lower extremity orthopaedic surgery
* Active joint or systemic infection, significant muscle paralysis, significant lower extremity or medical comorbidity that could alter the effectiveness of the surgical intervention (e.g. polymyalgia rheumatica)
* Unable to speak or read English/French
* Unable or unwilling to be followed for 1 year or complete functional testing
* Presence of chronic pain syndromes
* History of pediatric hip disease (i.e. Slipped Capital Femoral Epiphysis, Legg-Calve-Perthes Disease)
* Ongoing litigation or compensation claims related to the hip (including Workers' Compensation)

Radiographic:

* Osteoarthritis greater than Tönnis Grade 1 on affected hip
* Lateral central edge angle \<19°
* Dysplasia in patients with broken Shenton line (i.e. Severe acetabular deformity present)

Study Location

Pan Am Clinic
Pan Am Clinic
Winnipeg, Manitoba
Canada

Contact Study Team

Primary Contact

Dan Ogborn, PhD

[email protected]
204-927-2829
Study Sponsored By
Panam Clinic
Participants Required
More Information
Study ID: NCT05280899