WALANT versus brachial plexus Block for Distal Radius Fracture Fixatio
Not Applicable
Not yet recruiting
- Conditions
- SurgeryAnaesthesia
- Registration Number
- PACTR202407490456486
- Lead Sponsor
- Mansoura university hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
both sex aged 18-75 years old,
- diagnosed with distal radius fracture, scheduled for surgical fixation (volar plating), and
- classified as class I , II and III according to the American Society of Anesthesiologists (ASA) physical status score.
Exclusion Criteria
- polytrauma patients
- patients refusing regional anesthesia
- bleeding diathesis, needle phobia, anxiety, peripheral vascular disease
- known hypersensitivity to any of the study medication.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms of WALANT in distal radius fracture fixation compared to brachial plexus blocks?
How does WALANT compare to brachial plexus block in terms of postoperative pain management and recovery outcomes for distal radius fractures?
Are there specific biomarkers that can predict patient suitability for WALANT versus brachial plexus block in orthopedic surgery?
What are the potential adverse events associated with WALANT and how do they compare to those of brachial plexus blocks in fracture fixation?
What are the current trends in local anesthetic techniques for distal radius fracture fixation, and how does this trial contribute to the field?