Actively Recruiting

Age: 18Years +
All Genders
ID05701592

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

Led by Konrad Malinowski MD · Updated on 2023-01-27

10

Participants Needed

1

Research Sites

52 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are evaluating the outcomes of Double-bundle Posterior Cruciate Ligament Reconstruction (DB-PCLR) for patients with Posterior Cruciate Ligament (PCL) tears. This observational study aims to assess whether DB-PCLR, which reconstructs both the anterolateral and posteromedial bundles of the PCL, can improve patient results compared to the single-bundle procedure. The study is led by Konrad Malinowski MD and focuses on patients with grade III symptomatic posterior instability. Participants will undergo the DB-PCLR procedure, which involves reconstructing both PCL bundles. The study monitors patients treated with this method to evaluate knee stability and function over time. There are no comparison groups, as this is an observational assessment of patients receiving DB-PCLR. During the study, participants will be followed up at 12 and 24 months after surgery. Researchers will assess knee posterior translatory stability using clinical tests such as the posterior sag, drawer, Lachman tests, and stress X-rays, as well as knee internal rotation stability. Functional outcomes will be measured using questionnaires like the International Knee Documentation Committee (IKDC) and the Knee injury and Osteoarthritis Outcome Score (KOOS). Additionally, retear rates and range of motion (ROM) will be evaluated. The study will provide detailed follow-up on knee function and stability for up to two years post-treatment.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • PCL tear with III grade symptomatic posterior instability confirmed clinically and radiologically
  • Full knee range of motion
Not Eligible

You will not qualify if you...

  • Active knee inflammation
  • Non-adherence to the study protocol
  • Fixed posterior drawer

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 1 week

Participants undergo double-bundle posterior cruciate ligament reconstruction (DB-PCLR) surgery and receive immediate post-operative care.

1 visit for surgery and immediate post-operative assessments

Post-operative Follow-up

Duration - 24 months

Participants are monitored for knee stability and functional recovery after surgery.

Visits at 12 months and 24 months post-surgery

Trial Site Locations

Total: 1 location

1

Artromedical Orthopaedic Clinic

Bełchatów, Łódź Voivodeship, Poland, 97-400

Actively Recruiting

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Research Team

K

Konrad Malinowski, MD PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Single-Bundle and Double-Bundle Posterior Cruciate Ligament Reconstructions: A Systematic Review and Meta-analysis of 441 Patients at a Minimum 2 Years' Follow-up.

Jorge Chahla, Gilbert Moatshe, Mark E Cinque...

https://pubmed.ncbi.nlm.nih.gov/28866340

Double-Bundle Posterior Cruciate Ligament Reconstruction in 100 Patients at a Mean 3 Years' Follow-up: Outcomes Were Comparable to Anterior Cruciate Ligament Reconstructions.

Robert F LaPrade, Mark E Cinque, Grant J Dornan...

https://pubmed.ncbi.nlm.nih.gov/29953296

Decreased Posterior Tibial Slope Does Not Affect Postoperative Posterior Knee Laxity After Double-Bundle Posterior Cruciate Ligament Reconstruction.

Andrew S Bernhardson, Nicholas N DePhillipo, Zachary S Aman...

https://pubmed.ncbi.nlm.nih.gov/30657698