ClinicalTrials.Veeva

Menu

Efficacy of Ultrasound Guided Erector Spinae Plane Block

M

Minia University

Status

Completed

Conditions

Postoperative Pain
Hemodynamic Instability
Patient Satisfaction
Regional Block

Treatments

Other: control
Procedure: Erector spinae plane block

Study type

Interventional

Funder types

Other

Identifiers

NCT04371705
Efficacy of ESPB

Details and patient eligibility

About

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

Full 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.

Enrollment

65 patients

Sex

All

Ages

25 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age18-70 .

  2. Both gender.

  3. ASA I-III .

Exclusion criteria

  1. patient refuse
  2. Drug allergy.
  3. Morbid obesity (BMI >40 kg/m2).
  4. Psychiatric disorder.
  5. Opioid dependence .

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

65 participants in 2 patient groups, including a placebo group

ESPB group
Experimental group
Description:
31 patients Will undergo ultrasound guided ESP block with 40 ml bupivacaine 0.25% (20 ml on each side).
Treatment:
Procedure: Erector spinae plane block
control group
Placebo Comparator group
Description:
31 patients anesthetized with the protocol followed by Minia University Hospital
Treatment:
Other: control

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems