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Combined Lumbar Erector Spinae Plane Block and Pericapsular Nerve Group Block in Patients Undergoing Hip Surgeries

NCT05930171 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2023-12-28

No results posted yet for this study

Summary

The investigators are going to evaluate the postoperative analgesic efficacy of combined LESPB and PENG block after hip surgeries.

Conditions

  • Lumbar Erector Spinae Plane Block
  • Pericapsular Nerve Group Block (PENG Block)

Interventions

PROCEDURE

Ultrasound guided L-ESPB and PENG block using Bupivacaine

Combined Lumbar Erector Spinae Plane Block and Pericapsular Nerve Group Block in Patients Undergoing Hip Surgeries

DRUG

Postoperative conventional analgesia in form of Acetaminophen

Postoperative conventional analgesia in form of acetaminophen 15 mg/kg/6hrs

Sponsors & Collaborators

  • Menoufia University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-02-01
Primary Completion
2023-08-01
Completion
2023-12-01

Countries

  • Egypt

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05930171 on ClinicalTrials.gov