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Anterior cruciate ligament tear treated by arthroscopic tension-relieving reconstrusction

The prospective randomized controlled trial for tension-relieving versus non-tension relieving at arthroscopic ACL reconstrusction for anterior cruciate ligament tear

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024005
Enrollment
Unknown
Registered
2019-06-22
Start date
2016-03-01
Completion date
Unknown
Last updated
2019-06-26

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

Conditions

Anterior cruciate ligament tear

Interventions

Control group:Routine method
Experimental group:arthroscopic tension-relieving reconstruction

Sponsors

The First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 45 years,male or female; 2. Primary anterior cruciate ligament injury; 3. ACL rupture combined with or without repair of meniscus injury; 4. normal contralateral knee joint

Exclusion criteria

Exclusion criteria: 1. If any of the following conditions exist in the ipsilateral knee: (1) Combined with tear of the posterior cruciate ligament of the knee; (2) Concomitant medial collateral ligament injury requiring repair; (3) Complex knee injury; 2. Previous history of knee injury; 3. previous surgical history of knee joint; 4. osteochondral injury above III degree; 5. Cannot be contacted by phone.

Design outcomes

Primary

MeasureTime frame
International Knee Disability Committee (IKDC) Survey;Lysholm score;Second-Look Arthroscopic Evaluation;Three-dimensional gait characteristics;—

Countries

China

Contacts

Public ContactLi Yanlin

The First Affiliated Hospital of Kunming Medical University

852387873@qq.com+86 15987186373

Outcome results

None listed

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