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Efficacy of Erector Spinae Plane Block Analgesia After Off Pump Cardiac Surgery

NCT05769309 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-03-19

No results posted yet for this study

Summary

In this study the investigators will investigate the efficacy of ESPB as a part of Enhanced recovery after surgery on postoperative analgesia and recovery criteria after off pump cardiac surgery.

Conditions

  • Postoperative Pain

Interventions

PROCEDURE

Erector spinae block

After induction, the patients will be administered bilateral Erector spinae block with 20 ml of 0.25 % bupivacaine

DRUG

Fentanyl

fentanyl boluses of 0.5-to-1 µg/kg titrated according to haemodynamic parameters.

Sponsors & Collaborators

  • Menoufia University

    lead OTHER

Principal Investigators

  • Islam M ElDesoky, MD · Menoufia University

  • AMAL G SAFAN, MD · Menoufia University

  • Abd-Elazeem A Elbakry, MD · Menoufia University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-22
Primary Completion
2023-10-10
Completion
2023-12-25

Countries

  • Egypt

Study Locations

More Related Trials

Entities

Drugs

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 NCT05769309 on ClinicalTrials.gov