A randomized clinical trial comparing intrathecal morphine and continuous erector spinae block for postoperative analgesia in living donors for liver transplantatio
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0004313
- Lead Sponsor
- Samsung Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Adult (=19 years old or >19 years old) American society
of anesthesiologist physical status I, II: healthy (I), controlled systemic
disease (II)
Exclusion Criteria
American society of anesthesiologist physical status higher
than III: uncontrolled systemic disease (III), severe systemic disease (IV),
death (V) Child (<18 years old or =18 years old) Old Age (=70 years old
or> 70 years old) Pregnancy Coagulopathy Unstable coronary artery disease,
congestive heart failure, arrythmia, cardiomyopathy Cerebrovascular disease
Systemic infection, infection at site of erector spinae plane block chronic
pain disorder Refusal to study Allergy to local anesthetics Psychiatric
disease
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method cumulative opioid consumption at 48 hours <br>postoperatively
- Secondary Outcome Measures
Name Time Method pain scores;cumulative opioid consumption;patient satisfaction with pain relief;quality of sleep;quality of recovery;catheter-related complications (disruption, infection, leakage, <br>migration);Time to first flattus;Time to first ambulation;postoperative nausea, vomiting, and pruritus;incidence of respiratory depression and post-dural puncture <br>headache;intraoperative remifentanyl consumption and surgical pleth <br>index;block performance time;block failure rate;pain characteristics and duration