Continuous Cryotherapy vs Ice Pack for ACL Surgery Recovery
Continuous compression cryotherapy
+ Conventional ice treatment
Anterior Cruciate Ligament Injuries+8
+ Knee Injuries
+ Leg Injuries
Supportive Care Study
Summary
Study start date: June 1, 2023
Actual date on which the first participant was enrolled.This study focuses on comparing two different methods of cold therapy to help patients recover after anterior cruciate ligament (ACL) reconstruction surgery. The goal is to see which method is more effective in reducing pain, swelling, and improving knee movement, while also assessing patient satisfaction. The study involves patients who have recently undergone ACL surgery, and understanding the best cold therapy method can help improve recovery outcomes and patient comfort during the critical first few days after surgery. Participants in the study are randomly assigned to either use ice packs or continuous compressive cryotherapy for three days following their surgery. The effectiveness of these treatments is measured by looking at pain levels using a Visual Analog Scale (VAS), the degree of knee swelling, the range of motion in the knee, and how satisfied patients feel with their recovery. This comparison helps determine which therapy provides better pain relief and recovery support, potentially guiding future postoperative care practices.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.72 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
University Medical Center, Ho Chi Minh city
Ho Chi Minh City, VietnamOpen University Medical Center, Ho Chi Minh city in Google Maps