A Randomized Clinical Trial

Status Completed

Clinical Trial Summary

Acute postoperative pain is a common problem faced by the patient after surgery, most frequently occurring in first 24 hours. Our primary objective was to assess pain score in first 24 hours in PECS block group undergoing mastectomies. Secondary objective was to observe morphine (opioids) and antiemetic consumption in post anesthetic care unit.

Clinical Trial Description

Design: Observer Blinded Randomized control trial.

Place and Duration: Department of Anesthesiology, Shaukat Khanum Memorial Cancer Hospital Lahore (SKMCH), from February 2017 to December 2017

Methods: 120 patients more than 18 years, ASA I and II, planned for unilateral elective modified radical mastectomy under general anesthesia were randomly assigned to receive either general anesthesia plus Pectoral Nerve I, II and serratus (PECS) block (n = 60) or general anesthesia alone (n = 60). Pain score at fixed intervals was measured using Numeric Pain Rating Score (NPRS) after surgery. ;

Study Design

Related Conditions & MeSH terms

Regional Anesthesia

Clinical Trial Details

NCT number	NCT03947463
Study type	Interventional
Source	Shaukat Khanum Memorial Cancer Hospital & Research Centre
Contact
Status	Completed
Phase	N/A
Start date	February 1, 2017
Completion date	March 1, 2018

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