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Analgesic Efficacy of Fascia Iliaca Compartment Block Compared With Intrathecal Nalbuphine for Hip Surgery Under Spinal Anesthesia: a Randomized Controlled Trial
Led by Ain Shams University · Updated on 2025-11-19
120
Participants Needed
1
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness of two pain control methods—fascia iliaca compartment block and intrathecal nalbuphine—in patients undergoing hip surgery with spinal anesthesia. The study compares how well these methods manage postoperative pain. This randomized controlled trial is sponsored by Ain Shams University and aims to measure the time until the first need for additional pain relief within 24 hours after surgery. Participants will receive one of three treatments: ultrasound-guided fascia iliaca compartment block combined with spinal anesthesia, intrathecal nalbuphine with spinal anesthesia, or spinal anesthesia alone. These treatments are administered during hip surgery under spinal anesthesia to assess their pain control effects. During the study, participants will be monitored for their pain levels and the time until they require rescue analgesia after surgery. The main outcome measure is the time to the first request for pain relief within the first 24 hours post-surgery. The study involves follow-up assessments to evaluate pain control effectiveness and safety throughout the recovery period.
CONDITIONS
Brief Title
Analgesic Efficacy of Fascia Iliaca Compartment Block Compared With Intrathecal Nalbuphine for Hip Surgery Under Spinal Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- American Society of Anesthesiologists (ASA) score ASA I or ASA II
- Age 21 years or older
- Body mass index less than 35 kg/m2
You will not qualify if you...
- Patient refusal to participate
- Known bleeding disorders (coagulopathy)
- Known peripheral nerve damage or neurological deficits
- Known allergy to study drugs
AI-Screening
AI-Powered Screening
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Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 24 hours after surgery
Participants receive either a fascia iliaca compartment block with spinal anesthesia, intrathecal nalbuphine with spinal anesthesia, or spinal anesthesia alone for hip surgery.
1 surgical procedure visit
Trial Site Locations
Total: 1 location
1
Ain-Shams University Hospitals
Cairo, Egypt
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How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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