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A comparative clinical study of autologous hamstringtendon single bundle reconstruction of anterior cruciate ligament graftswith and without high strength braided wire

A comparative clinical study of autologous hamstringtendon single bundle reconstruction of anterior cruciate ligament graftswith and without high strength braided wire

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086183
Enrollment
Unknown
Registered
2024-06-26
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-08

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:Pass two tendons through the Endobutton loop, fold the tendons into four strands, and pull them upwards through the tibial tunnel, joint cavity, and femoral tunnel
experimental group:Thread two tendons and non absorbable polyethylene braided tape through the Endobutton loop, tie a high-strength non absorbable polyethylene braided tape in a knot around the loop,

Sponsors

Shunde Heping Surgery Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? Age between 18 and 60 years old, regardless of gender ? Patients diagnosed with anterior cruciate ligament injury and requiring anterior cruciate ligament reconstruction surgery have a PSA of less than 12 degrees; Pivot shifs is less than level 1 ? The injury is located in the knee joint and there are no other serious joint diseases ? The patient has clear awareness and can cooperate with the doctor to complete surgical treatment ? Patients and their families sign informed consent forms and are willing to participate in this study

Exclusion criteria

Exclusion criteria: ? Simultaneous surgical reconstruction is required for combined collateral ligament or posterior cruciate ligament injuries ? Complicated with other serious diseases, such as cardiovascular, liver, kidney and other important organ dysfunction, diabetes, etc ? Pregnant and lactating women ? Individuals with mental illness or unclear consciousness who are unable to cooperate with doctors to complete surgical treatment ? Patients and their families are unwilling to participate in this study

Design outcomes

Primary

MeasureTime frame
Lysholm score;IKDC score;Tegner score;The incidence of front drawer test;

Secondary

MeasureTime frame
Complications;

Countries

China

Contacts

Public ContactQuan Yu

Shunde Heping Surgery Hospital

190822194@qq.com+86 159 8998 9549

Outcome results

None listed

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