Ignite Creation Date:
2024-07-17 @ 11:25 AM
Last Modification Date:
2024-10-26 @ 3:33 PM
Study NCT ID:
NCT06483607
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-07-03
First Post:
2024-06-25
Brief Title:
Comparison of M-TAPA and TAP Blocks on Postoperative Analgesia in Laparoscopic Inguinal Hernia Surgeries
Sponsor:
Cumhuriyet University
Organization:
Cumhuriyet University
Study Overview
Official Title:
Comparison of the Analgesic Effects of Modified Thoracoabdominal Nerve Block Through Pericondrial Approach M-TAPA and Transversus Abdominis Plane TAP Block in Laparoscopic Inguinal Hernia Surgeries
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-07
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:
The goal of this study is to compare the analgesic efficacy of M-TAPA block and TAP block in patients undergoing laparoscopic inguinal hernia surgeries
Detailed Description:
There will be three randomized groups Group Control no any block n30 Group M-TAPA n30 Group TAP n30 All patients will have standard general anesthesia Group M-TAPA patients will receive bilateral M-TAPA block with 025 bupivacaine total volume of 40 ml Group TAP patients will have bilateral lateral-TAP block with 025 bupivacaine total volume of 40 ml All blocks will be performed at the end of the surgery before awakening the patients All patients in the study will receive 50 mg dexketoprofen and 1 gr paracetamol intravenos iv 10 minutes prior to skin closure All patients will have ibuprofen 3x400 mg in postoperative 24 hours maximum dose 1200 mgday Numerical rating scale NRS will be used to assess postoperative pain on 1st 6th 12th 18th and 24th hour after the surgery 50 mg tramadol will be administered as a rescue analgesic in all patientsTotal tramadol consumption will be calculated
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