A Randomized Controlled Trial: Comparison of One-Per-Mil Tumescent Technique and Tourniquet in Surgery for Post-Burn Hand Contracture in Creating Clear Operative Field and Assessment of Final Functional Outcome
Not Applicable
Completed
- Conditions
- postburn hand contractureSurgery - Surgical techniquesInjuries and Accidents - Burns
- Registration Number
- ACTRN12621000569808
- Lead Sponsor
- Theddeus Octavianus Hari Prasetyono, MD, PhD
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
Patients aged 5-65 years, who are otherwise healthy, with post-burn hand deformity who will undergo contracture release in Cipto Mangunkusumo Hospital, Jakarta, Indonesia
- Patients who give informed consent to participate in the research
Exclusion Criteria
- Patients with hematologic disorders, peripheral vascular disorders, diabetes mellitus, hypertension, liver diseases, and rheumatic diseases
- Patients who are smoking except those who are willing to stop the smoking habit for at least two weeks before surgery
- Patients who consume anti-coagulant or anti-thrombotic medications, such as heparin, aspirin, clopidogrel, and warfarin
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The clarity of operative field.[The surgery will be video-recorded and three independent assessors will assess the clarity of operative field through the surgery video. The assessors will evaluate the first 15 minutes of the surgery continuously. It is continued by evaluating the first 10-minute of each hour of the surgery (every 10 minutes for each hour of surgery). All of the timepoints are accounted for the assessment.];-Total active movement of the hand assessed using goniometer<br>[At least 3 months postoperatively];Total passive movement of the hand assessed using goniometer[At least 3 months postoperatively]
- Secondary Outcome Measures
Name Time Method