Ignite Creation Date:
2024-05-06 @ 3:47 PM
Last Modification Date:
2024-10-26 @ 1:56 PM
Study NCT ID:
NCT04751552
Status:
COMPLETED
Last Update Posted:
2023-09-13
First Post:
2020-10-14
Brief Title:
Erector Spinae Block for Thoracoscopic Surgery
Sponsor:
St Antonius Hospital
Organization:
St Antonius Hospital
Study Overview
Official Title:
Effect of Erector Spinae Plane Block on Postoperative Pain Intensity in Patients Undergoing Thoracoscopic Surgery a Randomized Clinical Trial
Status:
COMPLETED
Status Verified Date:
2023-09
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:
This randomized clinical trial compares the effects of the erector spinae plane block with levobupivacaine and 09 saline on postoperative pain intensity and opioid consumptions following thoracoscopic pulmonary surgery
Detailed Description:
Sixty patients planned for thoracoscopic pulmonary surgery are randomly assigned to an erector spinae plane block ESPB with levobupivacaine intervention group or 09 saline control group ESPB is performed under general anaesthesia before surgery
Postoperative pain medication incudes acetominophen NSAIDs en parenteral morphine patient controlled analgesia
Following surgery pain intensity numeric rating scale is registered at the recovery ward one hour after surgery Furthermore pain intensity is registered 248 12 hours after the operation On the first postoperative day pain intensity is registered at 800 ocock AM and 800 oclock PM Opioid consumption is registered as a second parameter of postoperative pain
Postoperative pain medication incudes acetominophen NSAIDs en parenteral morphine patient controlled analgesia
Following surgery pain intensity numeric rating scale is registered at the recovery ward one hour after surgery Furthermore pain intensity is registered 248 12 hours after the operation On the first postoperative day pain intensity is registered at 800 ocock AM and 800 oclock PM Opioid consumption is registered as a second parameter of postoperative pain
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