A prospective comparison outcome between standard PCL reconstruction and PCL reconstruction with suture augmentation: A multi-center randomized-controlled trial

Phase 4

• Conditions: PCL injured knee patients; PCL reconstruction; PCL reconstruction with internal bracing

• Registration Number: TCTR20220303001
• Lead Sponsor: Thai Orthopedic Society for Sports Medicine (TOSSM)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-03-03
• Study Completion: 2023-03-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: nknown
• Sex: All
• Target Recruitment: 130

Inclusion Criteria

1.PCL injured patients using Posterior drawer test gr. III or confirm diagnosis by MRI
2.Performed the Side-to-side posterior tibial translation difference from normal contra-lateral knee more than 8-12 mm. via PCL Stress Radiographs in the kneeling technique
3.Performed PCL stress radiographs without pain
4.Understand well in Thai language and can made self-decision

Exclusion Criteria

1.Multiligamentous injury knee
2.Contralateral knee injury or bilateral knee laxity
3.Neurovascular injury of the affected knee
4.Previous knee surgery
5.Previous significant lower extremities injury or pathology
6.High risk of osteoporosis
7.Inflammatory arthritis
8.Corticosteroid used more than 4 weeks
9.Unfit to surgery
10.Knee osteoarthritis more than The Kellgren and Lawrence system grade 1

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Side to side difference 3, 6, 12 months milimeter

Secondary Outcome Measures

Name	Time	Method
ROM of knee 3, 6, 12 months degree,KOOS score 3, 6, 12 months scale,IKDC score 3, 6, 12 months scale,Lysholm score 3, 6, 12 months scale