Adding pericapsular nerve group (PENG) block for postoperative pain relief following elderly hip fracture surgery: A prospective randomized controlled trial.
Phase 4
Completed
- Registration Number
- TCTR20220622003
- Lead Sponsor
- /A
- Brief Summary
Pain score 12 hours after hip surgery of FICB+PENG block patients group was significantly lower than FICB only group . The FICB+PENG block patients group felt significantly less pain after sitting up for the first time when compared with FICB only group .
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
1. 65+ years old
2.ASA classification I-III
Exclusion Criteria
Alzheimer patients, incapable of pain level description, allergic history of bupivacaine, paracetamol, morphine, prohibition against spinal cord anesthesia and FICB and/or PENG block, pre-existing ailments such as heart failure, irregular acute heart pain, chronic obstructive lung disease, cerebrovascular disease and terminal chronic kidney failure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain score 12 hours Numerical rating scale
- Secondary Outcome Measures
Name Time Method Postoperative pain score 24 hours Numerical rating scale,Postoperative pain score 48 hours Numerical rating scale,Morphine consumption 48 hours Total morphine requirement,Time to first sitting without pain within 48 hours after end of the intervention Time,Time to first morphine requirement within 48 hours after end of the intervention Time,Complications such as nausea, vomiting, dizziness, respiratory depression within 48 hours after end of the intervention questionnaire interview