Cross Bracing Protocol Versus Surgery for Acute Anterior Cruciate Ligament Rupture

Recruiting N/A Interventional Study
Anterior Cruciate Ligament Rupture
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
16 – 40
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
180 (estimated)
Sponsor
University of Melbourne · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
The aim of the EMBRACE clinical trial is to compare outcomes (knee pain, symptoms, function and quality of life) between people with anterior cruciate ligament (ACL) rupture who are managed with either a novel bracing protocol (Cross Bracing Protocol), or with ACL reconstruction surgery. The main question that the trial aims to answer is: In individuals with acute ACL rupture, is management with …
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Aged 16 to 40 years; * Have a primary and acute ACL rupture (complete tear) confirmed by MRI scan; * At least moderately active before the ACL injury (a score of 5 to 10 on the Tegner Activity Scale before the injury); * Willing and able to give informed consent and participat…
Contacts

EMBRACE study co-ordinator

+613903 53027

embrace-study@unimelb.edu.au

CONTACT