The analgesic efficacy of Erector Spinae Plane Block in patients undergoing Laparoscopic Bariatric Surgery : A randomized controlled trial
Phase 2
Recruiting
- Conditions
- bariatric surgery, morbid obesityerector spinae plane block,postoperative pain,pain,bariatric surgery,quality of recovery
- Registration Number
- TCTR20220523001
- Lead Sponsor
- Ratchadapiseksompotch Research Fund
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
1. patients aged 18 years or above, scheduled for laparoscopic bariatric surgery at King Chulalongkorn Memorial Hospital
2. American society of Anesthesiologist (ASA) physical status class 1-3
3. Participant is willing and able to give informed consent for participation in the study
Exclusion Criteria
1. Hypersensitivity to the drugs used in the study
2. Unable to perform the Thai QoR-35 questionnaire and use numerical rating scale (NRS)
3. Chronic opioid use
4. Unable to use patient controlled analgesia (PCA) device
5. Denie to recived ESPB
6. Infection at the puncture site
7. Require postoperative ICU admission and remain intubation
8. The presence of coagulopathy, hepatic, renal, or uncontrolled cardiovascular/respiratory disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The cumulative 24-hour postoperative morphine consumption 24-hour postoperative Cumulative 24-hour postoperative morphine consumption(morphine equivalent)
- Secondary Outcome Measures
Name Time Method Postoperative pain assessment at 0, 1, 6, 12, 18 and 24 h after surgery Numerical rating scale at rest and on motion ,Intraoperative and PACU fentanyl consumption Intraoperative and at PACU Anesthetic record,Time to the first postoperative morphine dose Postoperative PCA device record ,Intraoperative desflurane consumption End of anesthesia Anesthetic machine record,Quality of Recovery 24-hour postoperative The Thai QoR-35 questionnaire,Side effect : nausea and vomiting 24-hour postoperative Patient's symptom and nurse record,Patient satisfaction score 24-hour postoperative Numerical rating scale from 5 to (-)5