Severe Acetabular Labral Injuries
Conditions
Interventions
Acetabular Labrum Debridement Group:None
Iliotibial Band Reconstruction Group:None
Hamstring Tendon Reconstruction Group:None
Sponsors
Peking University Third Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: 1. Age: Adults aged 18-50 years 2. Patients with chronic pain in the hip joint, with poor results of conservative treatment such as exercise adjustment/topical drugs/oral non-steroidal anti-inflammatory drugs for more than 3 months 3. Patients with severe labral injury (labral absence or width < 3 mm, labral parenchymal degeneration with cyst formation, extensive labral calcification) confirmed by hip MRI, who are not expected to be repaired with sutures before surgery, and need to be cleaned/reconstructed 4. The patient voluntarily participates in the clinical trial, signs the informed consent form, and is able to cooperate with the completion of clinical follow-up.
Exclusion criteria
Exclusion criteria: 1. Those who have participated in clinical trials of other drugs or medical devices within the last 6 months 2. History of previous ipsilateral hip surgery 3. Patients who underwent bilateral surgery at the same time 4. Patients with moderate to severe hip dysplasia: there are signs of insufficient acetabular coverage such as LCEA 15°; 5. Patients with moderate to severe osteoarthritis: Tönnis grade > 2 6. Combined with hip-specific synovitis (such as rheumatoid synovitis, gouty synovitis, pigmented villonodular synovitis, etc.)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Modified Harris Hip Score (MHHS);International Hip Outcome Tool-12(iHOT-12);Patient-Reported Outcome (PRO); Visual Analog Scale (VAS);MRI imaging criteria;Knee Injury and Osteoarthritis Outcome Score (KOOS) ; | — |
Countries
China
Contacts
Public ContactHongjie Huang
Peking University Third Hospital
Outcome results
None listed