Clinical trial No longer in our active list Interventional Ages 16 to 60

Rehabilitation options for patients with acute PCL injuries

Official title: Kneelaxity and Self-reported Knee Function After Rehabilitation With the Use of Dynamic Kneeorthosis for Patients With Acute Isolated Posterior Cruciate Ligament Injury: A Randomized Controlled Trial

Run by Oslo University Hospital · NCT02974205 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.

This study is testing different rehab methods for people with recent PCL injuries to see which one helps their knee feel more stable and function better.

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Quick facts

Study typeInterventional
Ages16 Years to 60 Years
SexAll
Enrollment80 (estimated)
SponsorOslo University Hospital
Academic / other
Locations2 sites (Lørenskog and 1 other locations)
Trial IDNCT02974205 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals aged 16-60 who have sustained an acute isolated PCL injury within the last 21 days.

Probably not a fit

Patients with additional knee ligament injuries, cartilage damage, or those who are unable to participate in rehabilitation may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effectiveness of different rehabilitation protocols for patients with acute isolated posterior cruciate ligament (PCL) injuries. It aims to determine if one rehabilitation method leads to better knee joint stability and improved patient-reported knee function compared to others. A total of 75 patients will be randomly assigned to different treatment groups and followed up at 3 and 12 months post-injury. The outcomes will be assessed using knee laxity measurements and subjective function scores.

Why it matters

Potential benefit: If successful, this study could lead to improved rehabilitation strategies for patients with acute PCL injuries, enhancing their recovery and knee function.

How similar studies have gone: While there is limited research specifically on PCL rehabilitation, similar studies on knee ligament injuries have shown promising results with structured rehabilitation protocols.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Acute isolated PCL injury : 0- 3 weeks ( maximum 21 days) from the initial injury
* Isolated PCL rupture (grade I, II and III)
* Patient age should be between 16-60 years ( with closed epiphyseal plate )
* Understood and accepted written consent

Exclusion Criteria:

* Injury to the ACL or other ligaments in the knee
* Extensive injury to the cartilage or meniscus , requiring repairs
* Unfit to understand or to sign consent
* History of alcohol or drug abuse in the past three years
* Current serious illness or injury that makes rehabilitation difficult.

Where it's running

  • Akershus University Hospital
    Lørenskog, Norway
    Recruiting
  • Oslo University Hospital
    Oslo, Norway
    Recruiting

Study contacts

  • Principal investigator: Lars Engebretsen, Dr. Med — Oslo University Hospital
  • Study coordinator: Ingrid Trøan, PT
  • Email: ingrid.troan@ous-hf.no
  • Phone: +479888593

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.