Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06553573
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-08-12
Brief Title:
Comparison of PSB and RIFPB Combination With PSB and ESPB Combination in Cardiac Surgery With Sternotomy
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Postoperative Analgesic Efficacy Comparison of a Combination of Superficial Parasternal Block PSB and Recto-intercostal Fascial Plane Block RİFPB Versus a Combination of Erector Spinae Plane Block ESPB and Superficial Parasternal Block PSB in Patients Undergoing Cardiac Surgery With Sternotomy
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 goal of this study is to compare the analgesic efficacy of the combination of PSB and RIFPB and the combination of PSB and ESPB in patients undergoing cardiac surgery with sternotomy
Detailed Description:
This study will consist of two randomized groups Group RIFPB n12 Group ESP n12 All patients will receive standard general anesthesia Group RIFPB patients will receive PSB and RIFPB with 025 bupivacaine total volume 60 ml bilaterally Group ESPB patients will receive PSB and ESPB with 025 bupivacaine total volume 60 ml bilaterally All blocks will be performed after induction of general anesthesia and before surgical incision All patients in the study will be given 50 mg dexketoprofen and 1 g paracetamol intravenously iv 10 minutes before skin closure Within the first 24 hours after surgery all patients will be given 3x1 g iv paracetamol and 2x50 mg dexketoprofen Numerical Rating Scale NRS will be used to assess postoperative pain at 1 6 12 18 and 24 hours All patients will receive morphine via a patient-controlled analgesia PCA device within 24 hours of surgery If pain score is 4 despite this protocol 50 mg tramadol iv maximum dose 300 mgday will be administered as rescue analgesia
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