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A retrospective cohort study evaluating alloscopic MPFL reconstruction combined with medial support band tightening for recurrent patellar dislocation

A retrospective cohort study evaluating alloscopic MPFL reconstruction combined with medial support band tightening for recurrent patellar dislocation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126549
Enrollment
Unknown
Registered
2026-06-11
Start date
2026-06-11
Completion date
Unknown
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent patellar dislocation

Interventions

Group of total arthroscopic MPFL reconstruction combined with medial support band tightening:None
Group of traditional MPFL reconstruction:None

Sponsors

The Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1.Undergoes total microscopic MPFL reconstruction combined with medial support band tightening or conventional MPFL reconstruction; 2.Patients undergoing reconstructive surgery were treated with autologous tendon grafts and screw fixation at the lateral femoral interface; 3.Scooter dysplasia is typed as Dejor A, B or C; 4.The duration of the injury is less than 6 weeks; 5.There was no significant joint degeneration or extra-articular deformity; 6.Rehabilitation according to a standard plan with complete postoperative follow-up data; 7.Gender is not a requirement and the age is 15-30 years.

Exclusion criteria

Exclusion criteria: 1.Combination of complete rupture of other knee ligaments (e.g. cruciate ligament, medial collateral ligament) and need for joint reconstruction; 2.Accompanied by a significant fracture (e.g., femoral condyle or tibial plateau fracture) or severe osteoarthritis; 3.This is a revision surgery; 4.Have a serious systemic disease (e.g., uncontrolled diabetes, hypertension, connective tissue disease, etc.); 5.Presence of a definite local infection (e.g., septic inflammation of the knee) or systemic infection prior to surgery; 6.Suffering from knee tumours, rheumatism, rheumatoid rheumatism, gout, tuberculosis and other diseases affecting the structure of the joint; 7.Those with severe allergic or rejection reactions to endoprosthetic materials, such as anchor staples, loop steel plates, sutures, etc; 8.Those with incomplete data or less than 24 months of follow-up; 9.Those deemed unsuitable by other doctors.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale;IKDC Knee Motion Level Score;Postoperative imaging evaluation (MRI);Tegner Knee Motion Level Score;Lysholm Knee Function Score;Range of motion of knee joint;

Secondary

MeasureTime frame
safety assessment;Operational Satisfaction Score;Complication rate;

Countries

China

Contacts

Public ContactZhu Weihong

The Second Xiangya Hospital of Central South University

zhuweihong@csu.edu.cn+86 731 85296112

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026