Assessment of Outcomes of Double-bundle Posterior Cruciate Ligament Reconstruction (DB-PCLR)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorKonrad Malinowski MD

About this trial

Double-bundle Posterior Cruciate Ligament Reconstruction (DB-PCLR) is becoming increasingly used alternative to the single-bungle PCLR. While more technically challenging, it seems to better improve patients' outcomes. Therefore, outcomes of DB-PCLR will be assessed and reported.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

PCL tear with III grade sympomatic posterior instability confirmed clinically and radiologically

full knee range of motion

Disqualifiers

active knee inflammation

non-adherence to the study protocol

fixed posterior drawer

Trial population

Patients after PCL tear with knee instability undergoing DB-PCLR

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • DB-PCLR

    Procedure/Surgery

    DB-PCLR with reconstruction of both PCL bundles: anterolateral and posteromedial bundle will be performed.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: Patients with PCL tear treated with DB-PCLR1 intervention

Trial outcomes

Primary outcomes

1

Knee posterior translatory stability - posterior sag test

Posterior sag test will be performed and outcome will be presented as present/ absent

Time frame
At the 12 month of the follow-up.
2

Knee posterior translatory stability - posterior drawer test

Posterior drawer test aided with Rollimeter will be performed and outcomes will be presented in milimeters

Time frame
At the 12 month of the follow-up.
3

Knee posterior translatory stability - posterior Lachman test

Posterior Lachman test aided with Rollimeter will be performed and outcomes will be presented in milimeters

Time frame
At the 12 month of the follow-up.
4

Knee posterior translatory stability - stress X-ray

Stress X-ray assessing posterior translatory stability of the knee will be performed and outcomes will be presented in milimeters

Time frame
At the 12 month of the follow-up.

Secondary outcomes

1

The functional assessment with the The International Knee Documentation Committee Questionnaire (IKDC)

Min of 0 max of 87 points, higher scores mean a better outcome

Time frame
At the 12 month of the follow-up.
2

The functional assessment with the The International Knee Documentation Committee Questionnaire (IKDC)

Min of 0 max of 87 points, higher scores mean a better outcome

Time frame
At the 24 month of the follow-up.
3

The functional assessment with the Knee injury and Osteoarthritis Outcome Score (KOOS)

Min of 0 max of 100 points, higher scores mean a better outcome

Time frame
At the 12 month of the follow-up.
4

The functional assessment with the Knee injury and Osteoarthritis Outcome Score (KOOS)

Min of 0 max of 100 points, higher scores mean a better outcome

Time frame
At the 24 month of the follow-up.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Konrad Malinowski MD

Lead sponsor

Artromedical Konrad Malinowski Clinic

Sponsor institution