Actively Recruiting

Phase Not Applicable
Age: 21Years +
All Genders
ID06818396

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

On this page

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

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

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

Actively Recruiting

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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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