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NCT05300854 Clinical Trial

Serratus Block Versus Paravertebral Block for Post Thoracotomy Pain Relief

Post Operative Pain Clinical Trial

Official title:
Serratus Anterior Plane Block Versus Paravertebral Plane Block for Post Thoracotomy Pain Relief: A Comparative Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05300854
Other study ID # soh-Med-22-2-23
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2019
Est. completion date August 1, 2020

Study information
Verified date March 2022
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This double-blinded, randomized controlled study was done on 60 patients older than 18 years undergoing thoracotomy. Patients were allocated into two equal groups (30 patients each). Group S: Standard anesthesia in addition to SPB. II. Group P: Standard anesthesia in addition to PVB.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date August 1, 2020
Est. primary completion date June 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patients more than 18 ys undergoing thoracotomy operation Exclusion Criteria: - morbid obesity (Body mass index > 40) - impossibility of anatomical structures US identification in a satisfactory way - opioids treatment before surgery or substance abuse, - sepsis and/or infection at the puncture sites

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Standard anesthesia in addition to serratus plane block
a US-guided SPB was performed after induction of general anesthesia with the patient lying supine.
• Standard anesthesia in addition to para-vertebral block
Standard anesthesia in addition to para-vertebral block

Locations
Country Name City State
Egypt Faculty of Medicine, Sohag University Sohag

Sponsors (1)
Lead Sponsor Collaborator
Sohag University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary prevention of post-operative pain reduction of visual analogue score 72 hours
Primary reduction of analgesic requirement 72 hours
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