Which nerve block wins for hip surgery pain?
NCT ID NCT06003738
First seen Aug 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This trial compares two types of ultrasound-guided nerve blocks—pericapsular nerve group (PENG) and fascia iliaca compartment block (FICB)—for pain relief after total hip replacement surgery. Adults aged 18 to 80 scheduled for hip replacement under spinal anesthesia will be randomly assigned to receive one of the two blocks. Researchers will measure pain levels over 24 hours, the amount of rescue pain medication needed, and how quickly patients can walk again. The goal is to see which block provides better pain control and faster recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Two types of ultrasound-guided nerve blocks: pericapsular nerve group (PENG) block and fascia iliaca compartment block (FICB)
- What this could lead to
- If one block proves better, it could lead to improved pain control and faster recovery for people undergoing hip replacement surgery.
- What could go wrong
- This is a small, early-stage comparison, and results may not apply to all patients. Nerve blocks carry risks like bleeding, infection, or nerve damage, though rare.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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68 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Sep 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age from 18 to 80 years. * Both sexes. * American Society of Anaesthesiologists (ASA) Physical Status II-III. * Scheduled for Total hip arthroplasty (THA) under spinal anesthesia. Exclusion Criteria: * Patients' refusal * Contraindications to spinal anesthesia or nerve blocks. * History of allergy to the medications used in the study. * Pregnancy. * Significant cognitive impairment.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ain shams University
Cairo, 11588, Egypt
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