A comparative study of the contribution of brachial plexus block in shunt creation surgery
Not Applicable
Recruiting
- Conditions
- End-stage renal failure
- Registration Number
- JPRN-UMIN000048147
- Lead Sponsor
- Seirei Hamamatsu General Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 75
Inclusion Criteria
Not provided
Exclusion Criteria
Patients in whom the effects of nerve block were poor (patients with severe pain in the operative field requiring intravenous analgesics or sedatives in addition to regional anesthesia, or patients who were converted to general anesthesia). Patients with complications from the administration of nerve block, such as pneumothorax or subclavian artery puncture. Patients on vasoconstrictors for poor circulation.
Study & Design
- Study Type
- Observational
- 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 molecular mechanisms underlie brachial plexus block efficacy in end-stage renal failure patients undergoing shunt surgery?
How does brachial plexus block compare to systemic analgesia in postoperative outcomes for hemodialysis shunt creation?
Are there specific biomarkers that predict optimal response to regional anesthesia in vascular access surgery for chronic kidney disease?
What adverse events are associated with brachial plexus block in patients with end-stage renal disease and how are they managed?
What combination analgesic strategies with brachial plexus block improve recovery in arteriovenous fistula creation for renal failure?