Quality of Recovery After Hip Fracture Surgery: US-guided PENG Block Versus FICB
Sponsored by University Tunis El Manar
About this trial
Last updated a year ago
Study ID
Chaima Debabi
Status
Completed
Type
Interventional
Phase
N/A
Placebo
No
Accepting
65+ Years
All
Not accepting
Healthy Volunteers
Trial Timing
Ended 3 years ago
What is this trial about?
Patients were randomly divided into two groups to receive either ultrasound-guided
pericapsular nerve group block (PENG group) or fascia iliaca compartment block (FICB
group), using 20 ml of 0.2% ropivacaine
What are the participation requirements?
Inclusion Criteria
- patients aged above 65 years
- patients with an american society of anesthesiologists physical status I to III
- patients undergoing hip fracture surgical repair
Exclusion Criteria
- patients with an american society of anesthesiologists physical status IV or more
- inability or refusal to sign informed consent
- contraindications for regional nerve block or spinal anesthesia
- impaired cognition or dementia