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The Safety and Effectiveness of PEEK Interference Screws in Anterior Cruciate Ligament Reconstruction

C

Central South University

Status and phase

Unknown
Phase 3

Conditions

PEEK Interference Screw; Fixation; Anterior Cruciate Ligament Reconstruction

Treatments

Device: Interference Screws

Study type

Interventional

Funder types

Other

Identifiers

NCT03342222
JMST-01

Details and patient eligibility

About

Anterior cruciate ligament (ACL) rupture is one of the most common injuries in sports medicine. ACL reconstructions are usually performed to restore the stability of knee joint and prevent the secondary meniscal and chondral lesions.

120 Subjects with ACL injury were randomly assigned to two groups for ACL reconstruction.Group one: tibial fixation with PEEK Interference Screws (Rejoin Hangzhou Martins Medical Equipment Co., Ltd.);Group two: tibial fixation with Biosure PK interference screw (Smith & Nephew plc). The subjects will be followed by 12 months after surgery for evaluations.Outcome measures included Lysholm score,IKDC, ADT,Lachman.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Voluntarily sign the informed consent form; Between the ages of 18 and 75; Positive ADT and positive Lachman test. Unilateral anterior cruciate ligament is confirmed by MRI (without posterior cruciate ligament injury or reconstruction); Tolerated for anterior cruciate ligament reconstruction surgery; Normal contralateral knee

Exclusion criteria

  1. Do not meet the diagnostic criteria of anterior cruciate ligament injury;
  2. With posterior cruciate ligament fracture at the same time;
  3. X-ray showed a significant degeneration of the knee (more than four degrees of cartilage injury);
  4. Knee flexion less than 90 degree;
  5. Abnormal body anatomy;
  6. Pregnant, breast-feeding or subjects who plan to become pregnant;
  7. Serious osteoporosis, malignant tumors;
  8. Allergic to implant materials;
  9. Patients with severe malnutrition who can not tolerate surgery;
  10. Severe coagulopathy, such as hemophilia;
  11. Immunodeficiency diseases, including those requiring long-term use of immunosuppressive agents;
  12. The injured knee has a wide range of skin diseases;
  13. Serious obese patients (BMI> 35);
  14. Patients with severe mental illness can not cooperate with postoperative rehabilitation and patients with severe cardiopulmonary disease can not tolerate surgery;
  15. Ipsilateral lower extremity received surgery within the past year;
  16. Has participated in any other clinical trial in the past three months;
  17. Can not comply with the requirements of the study;
  18. Those who the investigator thinks they are inappropriate.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

120 participants in 2 patient groups

PEEK Interference Screws
Experimental group
Description:
PEEK Interference Screws provided by Ruijin Hangzhou Martins Medical Equipment Co., Ltd.
Treatment:
Device: Interference Screws
Biosure PK interference screw
Active Comparator group
Description:
Biosure PK interference screw from Smith \& Nephew plc.
Treatment:
Device: Interference Screws

Trial contacts and locations

1

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Central trial contact

Xi He, MD

Data sourced from clinicaltrials.gov

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