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ACL reconstruction comparing single bundle on the femur plus double bundle on the tibia and the traditional single bundle: A prospective randomized study

ACL reconstruction comparing single bundle on the femur plus double bundle on the tibia and the traditional single bundle: A prospective randomized study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013469
Enrollment
Unknown
Registered
2017-11-21
Start date
2016-07-01
Completion date
Unknown
Last updated
2017-11-27

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

Conditions

Ligaments injury and reconstruction

Interventions

Group A:ACL reconstruction with femoral single bundle and tibial double bundle
Group B:ACL reconstruction with traditional single bundle

Sponsors

Department of Sports Medicine in Sun Yat-sen Memorial Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Patients with ACL ruptures were diagnosed by knee MRI or arthroscopy; (2) 18-45 years old; (3) No gender preference; (4) Signing informed consent form.

Exclusion criteria

Exclusion criteria: (1) With knee osteoarthritis, articular cartilage injury, collateral ligament damage, posterior cruciate ligament damage, intra-articular fracture and other diseases; (2) Vascular injury or venous thrombosis was confirmed by preoperative conventional lower limb vein color ultrasound examination; (3) Nerve injury existed in the side lower limb; (4) Blood routine, heart, lung, liver, kidney function were obviously abnormal, compensatory function was insufficient, or existence of serious systemic disease; (5) Patients with neurological, mental system disorders, pregnant or lactating women, or those unsuitable for operation with a revelant disease history and serious organic disease; (6) Do not agree to the random allocation of reconstruction methods; (7) Participated in other clinical studies within three months; (8) Any situations the researchers believe that the cases should be excluded.

Design outcomes

Primary

MeasureTime frame
Knee subjective function evaluation;Knee stability evaluation;Knee motion function assessment;Imageological examination;

Countries

China

Contacts

Public ContactLi Weiping

Department of Sports Medicine in Sun Yat-sen Memorial Hospital of Sun Yat-sen University

lwp63@163.com+86 13802928802

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026