Viewing Study NCT06584981



Ignite Creation Date: 2024-10-26 @ 3:39 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06584981
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-08-20

Brief Title: Effect of PECS II Parasternal and Serratus Plane Blocks on Postoperative Pain in MIDCAB Surgery
Sponsor: None
Organization: None

Study Overview

Official Title: Effect of PECS II Parasternal and Serratus Plane Blocks on Postoperative Pain in MIDCAB Surgery
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: AIM It was aimed to evaluate the effectiveness of pectoral nerve block PECS II parasternal and serratus plane blocks in postoperative analgesia in minimally invasive cardiac surgery MIDCAB

INTRODUCTION The frequency of minimally invasive cardiac surgery has increased in recent years With this method Coronary artery bypass graft CABG operations can be performed without sternotomy It is a beneficial method for early postoperative mobilization early recovery and better aesthetic appearance Since there is a surgical intervention between the ribs pain control is important in these patients

METHOD In the preoperative evaluation of patients planned for CABG PECS II parasternal and serratus plane blocks are routinely recommended for postoperative pain control Consent for the procedure is obtained from patients who accept this procedure After induction and before the surgical incision these block applications are performed under sterile conditions under the guidance of ultrasonography Standard intravenous analgesic agents are applied to our patients who do not accept block applications The hospital core system files of our patients who underwent cardiac surgery with minimally invasive intervention in our hospital between January 1 2021 and December 31 2021 will be scanned retrospectively Patients with and without block application will be divided into two groups From our patients files Demographic data extubation time drain site and incision site pain at the 1st 2nd 4th 12th 24th 48th and 72nd hours after extubation will be noted In addition it will be noted whether there is a need for additional rescue analgesia in cases where block is performed The data obtained will be evaluated statistically and the results will be published in national or international scientific journals
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None