Viewing Study NCT06469073



Ignite Creation Date: 2024-07-17 @ 11:42 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06469073
Status: RECRUITING
Last Update Posted: 2024-06-21
First Post: 2024-06-16

Brief Title: Ultrasound-guided Modified Transversus Thoracic Muscle Plane Block and Erector Spinal Muscle Plane Block in Heart Valve Replacement Surgery With Median Incision
Sponsor: Le Yu
Organization: Shanghai East Hospital of Tongji University

Study Overview

Official Title: Ultrasound-guided Modified Transversus Thoracic Muscle Plane Block and Erector Spinal Muscle Plane Block in Heart Valve Replacement Surgery With Median Incision
Status: RECRUITING
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Sternum midline incision can offer better view under open-heart surgery and bigger operating space and therefore it has been widely used in most cardiac surgery If an event of urgency occurs it takes on a more important role than infrasternal small incision However sternum midline incision may cause serious pain and aggravates stress response and therefore patients are often reluctant to cooperate to cough which exerts adverse effect on postoperative rehabilitation and even causes serious complications such as pulmonary inflammation myocardial infarction and heart failure Thus the relief of pain and better perioperative analgesia are very important for these patients Transversus thoracic muscle planeTTMP block and erector spinal muscle planeESP block are used in open heart surgery currently and they can provide good analgesia This study aimed to investigate the hemodynamic stability total amount of analgesic use perioperative pain stress response postoperative complication and recovery in patients receiving TMP and ESP
Detailed Description: None

Study Oversight

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