Pericapsular Nerve Group and Lumbar Erector Spinae Plane Blocks for Geriatrics Undergoing Total Hip Arthroplasty

NCT06904703 · tracked via the Priya Life Science Egypt tracker

Sponsor

Tanta University

Phase

Not applicable

Started

2024-12-01

Last updated

2025-04-01

Condition(s) studied

Pericapsular NerveLumbar Erector Spinae Plane BlocksGeriatricsTotal Hip ArthroplastyGeneral Anesthesia

Investigational drug(s) / intervention(s)

General anesthesia →Bupivacaine 0.5% →Bupivacaine 0.5% →

General anesthesia: Patients will receive general anesthesia.

Bupivacaine 0.5%: Patients will receive general anesthesia and erector spinae plane block.

Bupivacaine 0.5%: Patients will receive general anesthesia and erector spinae plane block with pericapsular nerve block.

Study summary

This study will be conducted to evaluate the effect of pericapsular nerve group and erector spinae plane block as adjuvants to general anesthesia in geriatrics undergoing total hip arthroplasty.

Eligibility

Sex

ALL

Min age

75 Years

Max age

—

Healthy volunteers

Inclusion Criteria: * Aged \>75 years. * Both sexes. * American Society of Anesthesiologists (ASA) classification I-III. * Undergoing total hip arthroplasty under general anesthesia. Exclusion Criteria: * Patient refusal. * Body mass index (BMI) \> 30 kg/m2. * Allergy to local anesthesia drugs. * Infection at the site of intervention. * Coagulopathies. * Preexisting advanced diseases of the kidney or liver.

Primary outcome measure(s)

Mean sevoflurane MAC to achieve bispectral index (BIS) values (45-55) — Intraoperatively
Sevoflurane will be adjusted to maintain a steady state with a BIS value in the range of 45-55 and will be fixed through the study period

Trial sites (1)

Facility	City	Region	Status
Faculty of Medicine	Tanta	Egypt	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06904703 on ClinicalTrials.gov ↗ ← All trials in Egypt