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A randomized controlled clinical study of Remnant-Tensioning ACL reconstruction versus standard ACL reconstruction for acute and subacute ACL injuries

A randomized controlled clinical study of Remnant-Tensioning ACL reconstruction versus standard ACL reconstruction for acute and subacute ACL injuries

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073813
Enrollment
Unknown
Registered
2023-07-21
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Anterior cruciate ligament injury

Interventions

Study group :Remnant- Tensioning ACL reconstruction
Control group:Standard ACL reconstruction

Sponsors

The Second People's Hospital of Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects voluntarily entered the study and signed an informed consent form 2. Had a clear history of trauma 3. Had less than 3 months between injury and surgery 4. Had a positive anterior drawer test and a positive Lachman test 5. ACL remnant was evaluated as Sherman I-II remnant with good synovial coverage under arthroscopy. 6. Remnant-Tensioning ACL reconstruction or standard ACL reconstruction were performed 7.The patient or the guardian could understand the purpose of the study and show adequate compliance with the study protocol

Exclusion criteria

Exclusion criteria: 1. Chronic ACL injury (time between injury and surgery >3 months) 2. ACL remnant was evaluated arthroscopically as Sherman ?-IV remnant or Sherman I-II remnant with poor synovial coverage 3. Previous knee surgery history 4. Multiple ligament injuries or fractures near the knee joint 5. Serious knee diseases or systemic diseases (?-IV osteoarthritis, rheumatoid arthritis, etc.)

Design outcomes

Secondary

MeasureTime frame
IKDC sore;Tegner Score;3.0T MRI;single-leg hop test;Proprioceptive assessment;Knee stability;

Primary

MeasureTime frame
Lysholm Score;

Countries

China

Contacts

Public ContactWeimin Zhu

The Second People's Hospital of Shenzhen

szhzwm@email.szu.edu.cn+86 135 7087 9119

Outcome results

None listed

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