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NCT05633329 Clinical Trial

Dual Injection ESPB Versus Single Injection ESPB for Laparotomies

Post Operative Pain Clinical Trial

Official title:
Comparison Between the Efficacy of Ultrasound Guided Single Injection Erector Spinae Plane Block Versus Dual Injection Erector Spinae Plane Block for Postoperative Pain in Patients Undergoing Abdominal Surgery: Randomized Clinical Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05633329
Other study ID # 474:10/2022
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 7, 2022
Est. completion date June 1, 2023

Study information
Verified date June 2023
Source Minia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate and compare the efficacy of single level injection erector spinae plane block versus double level injection Erector spinae plane block in laparotomies

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date June 1, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: 1. Age18-60. 2. Both genders. 3. abdominal surgery. 4. ASA I-III. Exclusion Criteria: 1. Drug allergy. 2. Morbid obesity (BMI >40 kg/m2). 3. Psychiatric disorder. 4. Opiod dependence. 5. patient refuse.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• single level
injection of 40 ml bupivacaine 0.25 at T8 (20 ml on each side)
• dual level
injection of 40 ml of bupivacaine 0.25 at two level T7 and T9 (10 ml on each level of both side)

Locations
Country Name City State
Egypt Minia University Minya Minia

Sponsors (1)
Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary first analgesic request time to request fentanyl 24 hours
Secondary resting visual analogue pain scale pain score at rest from 0-10 which 0 mean no pain and 10 the worst pain 24 hours
Secondary dynamic visual analogue pain scale pain score at movement (cough) from 0-10 which 0 mean no pain and 10 the worst pain 24 hours
Secondary analgesic consumption total fentanyl required first day postoperative 24 hours
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