Comparison of the results of anteromedial and anterolateral tibial tunnel methods in posterior cruciate ligament reconstructio

Not Applicable

Recruiting

• Conditions: Rupture of the posterior cruciate tendon.; Other spontaneous disruption of posterior cruciate ligament of knee; M23.62

• Registration Number: IRCT20120215009014N472
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 36

Inclusion Criteria

Age of 18 to 65 years
Rupture of the posterior cruciate tendon

Exclusion Criteria

Coagulopathy disorder

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Average pain score. Timepoint: In the fourth and eighth weeks and the third month after surgery. Method of measurement: Using a visual analog scale (VAS).;The average time to return to daily activities. Timepoint: In the fourth and eighth weeks and the third month after surgery. Method of measurement: By taking a history.;The average range of motion limitation. Timepoint: In the fourth and eighth weeks and the third month after surgery. Method of measurement: Using the Lysholm Knee Scoring Scale.

Secondary Outcome Measures

Name	Time	Method
Hematoma. Timepoint: In the fourth and eighth weeks and the third month after surgery. Method of measurement: With clinical examination.