Ignite Creation Date:
2024-05-06 @ 7:26 PM
Last Modification Date:
2024-10-26 @ 3:07 PM
Study NCT ID:
NCT06017401
Status:
COMPLETED
Last Update Posted:
2024-03-06
First Post:
2023-08-20
Brief Title:
Oblique Subcostal Transversus Abdominis Plane Block Versus Transmuscular Quadratus Lumborum Block for Pain Management in Laparoscopic Gynecological Surgery
Sponsor:
Uludag University
Organization:
Uludag University
Study Overview
Official Title:
Comparison of The Effect of Oblique Subcostal Transversus Abdominis Plane Block and Transmuscular Quadratus Lumborum Block on Postoperative Analgesia and Quality of Recovery in Patients Undergoing Laparoscopic Gynecological Surgery
Status:
COMPLETED
Status Verified Date:
2024-03
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:
Laparoscopic gynecological surgery causes postoperative painThe primary objective of this study is to compare the effect of ultrasound US-guided oblique subcostal transversus abdominis plane block OSTAP on 24-hour total analgesic consumption with transmuscular quadratus lumborum block TQLB
Detailed Description:
Patients between the ages of 18-65 who will undergo laparoscopic gynecological surgery American Society of Anesthesiologists ASA class I-II-III Body Mass Index BMI in the range of 18-25 kgm² and who will use 3 or 4 trocar for surgery will be included in the study Patients will be randomized into two groups OSTAP block will be performed for OSTAPB group and TQL block will be performed for TQLB group Patients will be administered postoperative 4x500 mg iv paracetamol as needed if Visual Analogue Scale VAS score is 4 or higher If the VAS score remains at 4 or higher 30 minutes after paracetamol administration 1 mgkg iv tramadol will be administered as a rescue analgesic with a daily maximum dose of 400 mg The primary outcome is to compare the total analgesic consumption within the first 24 hours after surgery The secondary outcome is to compare the time to the first postoperative analgesic requirement VAS scores at rest and on movement and assess the impact of these two blocks on the quality of recovery using the QOR-15 scale
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