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

Comparison of the results of anteromedial and anterolateral tibial tunnel methods in posterior cruciate ligament reconstruction: a randomized clinical trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120215009014N472

Enrollment

Registered

2023-05-03

Start date

2023-05-22

Completion date

Unknown

Last updated

2023-05-29

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

Conditions

Rupture of the posterior cruciate tendon. Other spontaneous disruption of posterior cruciate ligament of knee

Interventions

Intervention 1: Intervention group 1: Arthroscopic surgery of the knee in order to reconstruct the posterior cruciate ligament of the knee by using single-strand Achilles graft through the medial ante

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age of 18 to 65 years Rupture of the posterior cruciate tendon

Exclusion criteria

Exclusion criteria: Coagulopathy disorder

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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

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

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alireza Naderi

Hamedan University of Medical Sciences

alirezanader97@gimail.com+98 81 3838 0572

Outcome results

None listed

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