Ignite Creation Date:
2024-05-06 @ 8:21 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06342076
Status:
COMPLETED
Last Update Posted:
2024-06-11
First Post:
2024-03-21
Brief Title:
Comparison of the Efficacy of Peripheral Nerve Blocks in Major Open Gynaecological Cancer Surgery
Sponsor:
Bakirkoy Dr Sadi Konuk Research and Training Hospital
Organization:
Bakirkoy Dr Sadi Konuk Research and Training Hospital
Study Overview
Official Title:
Comparison of the Efficacy of Subcostal Transversus Abdominis Plane Block and Rectus Sheath Block for Postoperative Analgesia in Major Open Gynaecological Cancer Surgery a Prospective Randomised Study
Status:
COMPLETED
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:
The aim of this prospective randomized study was to compare the effectiveness of subcostal transversus abdominis plane block or rectus sheath block applied in addition to posterior transversus abdominis plane block for postoperative analgesia in major gynecological cancer surgeries
The main questions it aims to answer are
Is subcostal transversus abdominis plane block more effective in postoperative analgesia Is there a difference in pain scores at 24 hours after surgery Since pain scores within the first 24 hours after surgery will be evaluated participants will be asked to give a value between 0 and 10 at certain time periods
The main questions it aims to answer are
Is subcostal transversus abdominis plane block more effective in postoperative analgesia Is there a difference in pain scores at 24 hours after surgery Since pain scores within the first 24 hours after surgery will be evaluated participants will be asked to give a value between 0 and 10 at certain time periods
Detailed Description:
This prospective randomized study was conducted at Başakşehir Çam and Sakura City Hospital in accordance with the Declaration of Helsinki After ethics committee approval decision no 2023-596 date 22112023 and written consent from all patients the study was conducted according to Consolidated Standards of Reporting Trials CONSORT guidelines In the study which included a total of 50 patients the patients were divided into two groups subcostal transversus abdominis plane block STAPB or rectus sheath block RSB Postoperative 24-hour VAS values opioid demand and administration amounts in intravenous patient-controlled analgesia presence of nausea and vomiting surgical complications and length of hospital stay were evaluated 6th hour 12th hour 24th hour
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