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The Arthroscopic Labral Excision or Repair Trial (ALERT)

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University of Oxford

Status

Unknown

Conditions

Acetabular Labrum Tear

Treatments

Procedure: Arthroscopic acetabular labral resection
Procedure: Arthroscopic acetabular labral repair

Study type

Interventional

Funder types

Other

Identifiers

NCT03257709
IRAS 184490

Details and patient eligibility

About

This study compares two established surgical treatments for acetabular labral tears. Patients will be prospectively recruited and randomised to either labral repair or debridement. All patients will be followed for 2 years after intervention with a primary outcome assessment at 6 months.

Full description

STUDY DESIGN

Study design This will be a two-arm randomised controlled parallel group superiority study and will take place in a hospital setting. Stratification will be performed for sex and age by means of a minimisation technique during randomisation for each subject entering the trial.

Study population:

Adults between 18 and 75 years of age diagnosed with symptomatic acetabular labral tears demonstrated on MRI arthrogram but without radiographic evidence of OA ie: Kellgren & Lawrence grade less than 2 randomly selected from the Nuffield Orthopaedic Centre outpatient clinics.

Arm 1 Arthroscopic acetabular labral repair.

Arm 2 Arthroscopic acetabular labral resection

48 patients per arm (total 96 patients) will be selected from outpatient clinics and the operative waiting list (pre-operative assessment clinics) at the Nuffield Orthopaedic Centre, Oxford. The surgeries will be conducted using routine instrumentation in use at the centre.

STUDY PROCEDURES

Recruitment

All patients will undergo surgery in accordance with established practice regardless of their treatment allocation. Arthroscopy will be performed using standard anterior and lateral portals for insertion of instruments. All patients will undergo arthroscopic evaluation of the entire joint. Subsequent procedures will vary according to treatment allocation:

  • Arm 1 - Labral Repair - acetabular labral tear will be identified and reattached using suture anchors until a stable repair is achieved. If evidence of FAI is present ie: a cam or pincer lesion is identified then this will be treated with osteochondroplasty (cam) or acetabular rim recession (pincer).
  • Arm 2 - Labral Resection - the acetabular labral tear will be identified and its' limits defined. The torn portion of labrum will be resected to a stable edge. As with arm 1 there will be treatment of FAI if identified.

Enrollment

96 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Willing and able to give informed consent for participation in the study.
  • Male or Female, aged between 18 and 75 years.
  • Symptomatic labral tear with evidence of labral tear on MRI.
  • No radiographic evidence of OA (Kellgren-Lawrence Grade < 2)

Exclusion criteria

  • Previous ipsilateral hip surgery
  • Irreparable labral tear
  • Previous fracture of femoral neck or acetabulum
  • Female patient who is pregnant
  • Established osteoarthritis (Kellgren-Lawrence ≥ 2)
  • Hip dysplasia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

96 participants in 2 patient groups

Arthroscopic acetabular labral repair
Active Comparator group
Description:
Acetabular labral tear will be identified and reattached using suture anchors until a stable repair is achieved. If evidence of FAI is present ie: a cam or pincer lesion is identified then this will be treated with osteochondroplasty (cam) or acetabular rim recession (pincer).
Treatment:
Procedure: Arthroscopic acetabular labral repair
Arthroscopic acetabular labral resection
Active Comparator group
Description:
The acetabular labral tear will be identified and its' limits defined. The torn portion of labrum will be resected to a stable edge. As with arm 1 there will be treatment of FAI if identified.
Treatment:
Procedure: Arthroscopic acetabular labral resection

Trial contacts and locations

1

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Central trial contact

Joanna S Burchall; John AJ Broomfield

Data sourced from clinicaltrials.gov

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