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Recruiting NCT04408885

Rehabilitation Treatment of Anterior Cruciate Ligament Rupture

— Observational ACL Injury

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Rehabilitation.
Who it may be relevant to
Registry conditions: ACL Injury. Basic parameters: 18 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose with this present study is to investigate the effect og a non-surgical regime in patients with an Anterior Cruciate ligament injury. The effect will be measured by patient reported outcome scores, level of function and how many of the patients are converting to operative treatment.

Interventions

  • Other Rehabilitation
    Non-surgical interventions to patients with an Anterior cruciate ligament injury. Rehabilitation regime is the regime provided by the physician at the rehabilitation clinic.

Primary outcome measures

  • Changes in patient reported outcome score (IKDC) [Time frame: Baseline - 2 Years]
Secondary outcome measures (3)
  • Changes in patient reported outcome score (KOOS) [Time frame: Baseline - 2 Years]
  • Changes in patient reported outcome score (KNEES-ACL) [Time frame: Baseline - 2 Years]
  • Changes in patient reported outcome score (TEGNER) [Time frame: Baseline - 2 Years]

Eligibility criteria

Inclusion criteria

  • Anterior cruciate ligament injury where rehabilitation regime is selected as treatment.

Exclusion criteria

  • Other knee ligament instability
  • Rheumatoid arthritis
  • Morbus Bechterews Disease

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Denmark · 1 center
  • Division of Sports Trauma, Palle Juul-Jensens Boulevard 99 — Aarhus N

Identifiers

NCT: NCT04408885 · Danish EC: 1-10-72-25-20

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗