A Study to Compare Two Different Managements After Ankle Surgery: Immediate and Delayed Weight-bearing.

Launched by ENTE OSPEDALIERO CANTONALE, BELLINZONA · Jun 10, 2020

Keywords

ClinConnect Summary

This clinical trial is looking at two different ways to manage recovery after ankle surgery for specific types of fractures known as lateral malleolus fractures. The researchers want to see if allowing patients to put full weight on their ankle right away, compared to waiting some time before bearing weight, can help them recover faster and achieve better function without causing more complications.

To be eligible for this study, participants need to be adults aged 18 to 70 who have a specific type of ankle fracture that requires surgery. They should be able to follow the study procedures and give their consent to participate. Throughout the trial, participants will receive guidance on their rehabilitation and monitor their recovery progress. It’s important to note that individuals with certain conditions, like more severe fractures or significant health issues, may not be able to take part in the study. This trial is currently recruiting, so if you or someone you know is interested, it may be a good opportunity to help advance treatment for ankle fractures.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Male and female adults
• • Age ranging from 18 to 70 years, included
• • Signed Informed Consent
• • Ankle fracture requiring surgical management classified as:1- Weber A fracture pattern (AO 44.A1, 44.A2, 44.A3) with or without association with a medial or posterior lesion/fracture or 2- Weber B fracture pattern (AO 44.B1, 44.B2, 44.B3) with or without association with a medial or posterior lesion/fracture
• • Willingness and ability to participate in the trial
• Exclusion Criteria:
• • Weber C fracture pattern
• • Bilateral fractures or fractures in other locations
• • Maissoneauve associated lesion
• • Body Mass Index \< 18.5 and ≥ 30
• • Metabolic diseases influencing fracture healing processes
• • Medical comorbidities precluding operative intervention
• • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, general physical problem of the participant, etc.
• • Inability or contraindications to undergo the investigated intervention
• • Other clinically significant concomitant disease states (e.g., renal failure, hepatic dysfunction, cardiovascular disease, etc.)
• • Pregnant women