Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06553560
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-12
Brief Title:
The Efficacy of PSB and Recto-intercostal Block Combination on Postoperative Pain in Patients Undergoing Cardiac Surgery Via Sternotomy Case Series
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Investigation of the Postoperative Analgesic Effect of the Combination of Superficial Parasternal Block PSB and Recto-IntercostalİC Fascial Plane Block in Patients Undergoing Cardiac Surgery Via Sternotomy Case Series
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:
The aim of this study was to investigate the effectiveness of the combination of Superficial Parasternal Block and Recto-Intercostal Fascial Plane Block in patient groups undergoing cardiac surgery via sternotomy by evaluating postoperative pain scores and analgesic consumption
Detailed Description:
Ten patients received a combination of parasternal block and recto-intercostal fascial plane block as an intervention Patients received bilateral parasternal block and recto-intercostal fascial plane block with 025 bupivacaine total volume 60 ml in the operating room before surgery All blocks will be performed after general anesthesia induction before skin incision All patients included in the study will be given 50 mg dexketoprofen and 1 g paracetamol intravenously iv 10 minutes before skin closure All patients will be given 3x1 g iv paracetamol and 2x50 mg dexketoprofen within the first 24 hours postoperatively Numerical rating scale NRS was used to assess pain at the 1st 6th 12th 18th and 24th hours after surgery Total morphine consumption was calculated using a patient-controlled analgesia PCA device Tramadol was planned as rescue analgesic medication maximum dose 300 mgday
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