Compression Therapy for Swelling Management Following Ankle Injury

Launched by NOVA SCOTIA HEALTH AUTHORITY · Jan 9, 2025

Keywords

ClinConnect Summary

This clinical trial is studying whether wearing a Bauerfeind ankle compression sleeve can help reduce swelling after an ankle injury or surgery. Swelling is a common issue that can occur after treatment, and managing it effectively is important to avoid complications and improve recovery. Currently, patients typically wear a walking boot after six weeks, which can lead to increased swelling. This study aims to compare the effects of using the compression sleeve alongside the walking boot to just using the boot alone to see if it helps patients recover better with less swelling and pain.

To participate in this trial, you need to be at least 18 years old and undergoing specific ankle surgeries or treatments at the Queen Elizabeth II Health Sciences Center. However, if you have complications with wound healing or certain health conditions, or if you can’t progress to a walking boot after six weeks, you may not be eligible. Participants can expect to have their swelling and pain monitored throughout the study, and the safety of the compression sleeve will also be evaluated. This trial is important as it could lead to better ways of managing swelling after ankle injuries or surgery, helping patients recover more smoothly.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Patients undergoing outpatient ankle, mid-foot or hindfoot arthrodesis, fracture surgery, or non-operative ankle fracture management at the Queen Elizabeth II Health Sciences Center.
• • Aged 18 or over
• Exclusion Criteria:
• • Patients undergoing other ankle procedures
• • Patients who have any signs of wound healing complications post-surgery
• • Patients who are unable to progress to walking boot and weight-bearing management at 6 weeks post operation/injury.
• • Patients with other co-morbidities that may create bias within the results (lymphedema, heart conditions etc.)
• • Patients who are unable to speak and read English, and/or in the opinion of the Principal Investigator are unable to provide fully informed consent.