PENG Block vs ESPB in Elderly Undergoing Hip Surgeries
Comparison Between the Ultrasound Guided Pericapsular Nerve Group Block and Erector Spinae Plane Block on Motor Power Postoperative in Elderly Patients Undergoing Total Hip Replacement Surgeries; A Randomized Controlled Trial
1 other identifier
interventional
56
0 countries
N/A
Brief Summary
To our knowledge, the comparison between the ultrasound-guided lumbar erector spinae plane block and the pericapsular nerve group block has not been investigated before in previous literature.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2025
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 19, 2025
CompletedFirst Posted
Study publicly available on registry
May 28, 2025
CompletedStudy Start
First participant enrolled
June 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedMay 29, 2025
May 1, 2025
5 months
May 19, 2025
May 28, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Motor power
The result of substraction of VAS from MRC at ipsilateral lower limb at the time of regaining of full motor power in the contralateral lower limb (delta).
24 hours postoperative
Study Arms (2)
PENG block
ACTIVE COMPARATORESPb
ACTIVE COMPARATORInterventions
Group LESBP: 28 patients will receive single shot LESPB after spinal induction. Group PENG: 28 patients will receive single shot PENG after spinal induction.
Group LESBP: 28 patients will receive single shot LESPB after spinal induction. Group PENG: 28 patients will receive single shot PENG after spinal induction.
Eligibility Criteria
You may qualify if:
- Both genders Type of surgery; unilateral elective total hip replacement. Physical status ASA I, II Age more than or equal 65 Years. Body mass index (BMI): \> 20 kg/m2 and \< 35 kg/m2.
You may not qualify if:
- Patient refusal. Patients with known sensitivity or contraindication to drugs used in the study (local anesthetics \& opioids).
- History of psychological disorders and/or chronic pain. Pre- existing peripheral neuropathies Coagulopathy. Infection of the skin at the site of needle puncture area.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
May 19, 2025
First Posted
May 28, 2025
Study Start
June 1, 2025
Primary Completion
November 1, 2025
Study Completion
December 1, 2025
Last Updated
May 29, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL