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Clinical Trials/NCT04371705
NCT04371705
Completed
Not Applicable

Efficacy of Ultrasound Guided Erector Spinae Plane Block in Patients Undergoning Abdominal Surgery

Minia University1 site in 1 country65 target enrollmentOctober 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hemodynamic Instability
Sponsor
Minia University
Enrollment
65
Locations
1
Primary Endpoint
Postoperative Total Fentanyl Requirement
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Thoracic epidural and paravertebral blocks are the most widely regional technique used for postoperative analgesia after surgery, but they are difficult to perform and carry a risk of serious complication. In this study, investigator asses the efficacy of ultrasound ESPB on intraoperative and postoperative hemodynamics and patient satisfaction

Detailed Description

This prospective, double-blinded, randomized, controlled study was conducted at the period from October 2018 to December 2019. Sixty adults' patients ASA I-III, their ages ranged from 25-60 years undergoing abdominal surgery under general anesthesia. Each patient assigned written informed consent before the block performance. Patients refused, known allergy to the used drugs, with history of coagulopathy, major organ failure and obesity (BMI\>40 kg/m2) were excluded from the study. Patients were randomly allocated into two equal groups by a computerized randomization table: ESPB group, and control group. The patient and the staff providing the postoperative care were blinded to the group assignment. ESPB group: Will undergo ESP block with 40 ml bupivacaine 0.25% (20 ml on each side) control group: anesthetized with the protocol followed by Minia University Hospital. Anesthetic technique was standardized for all patients.

Registry
clinicaltrials.gov
Start Date
October 15, 2018
End Date
December 1, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Minia University
Responsible Party
Principal Investigator
Principal Investigator

Hassan Mokhtar Elshorbagy Hetta

assistant lecturarl

Minia University

Eligibility Criteria

Inclusion Criteria

  • Both gender.
  • ASA I-III .

Exclusion Criteria

  • patient refuse
  • Drug allergy.
  • Morbid obesity (BMI \>40 kg/m2).
  • Psychiatric disorder.
  • Opioid dependence .

Outcomes

Primary Outcomes

Postoperative Total Fentanyl Requirement

Time Frame: 24 hours

The total amount of postoperative fentanyl in milligram

Secondary Outcomes

  • Time of First Post Operative Analgesic Request(24 hours)
  • heart rate (HR)(24 hours)
  • mean arterial pressure (MAP )(24 hours)

Study Sites (1)

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