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Postoperative analgesic effect of transabdominis plane block patients undergoing open abdominal aortic surgery; a randomized controlled trial

Postoperative analgesic effect of transabdominis plane block patients undergoing open abdominal aortic surgery; a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009160
Enrollment
86
Registered
2024-02-02
Start date
2024-03-24
Completion date
Unknown
Last updated
2024-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : 1) Transversus abdominis plane block : After completing the surgery, just before the end of anesthesia, use ultrasound in a supine position to check the inside of the transversus a

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Persons undergoing open surgery on the abdominal aorta for reasons such as correction of abdominal aortic aneurysm or bypass surgery of the abdominal aorta due to occlusion of the descending artery. - ASA physical status II, III based on the American Society of Anesthesiologists - Those who agree to the clinical trial and sign the subject consent form

Exclusion criteria

Exclusion criteria: - American Society of Anesthesiologists physical status (ASA physical status) IV or higher - Children under 18 years of age, adults over 80 years of age - pregnant woman - Patients with serious blood coagulation disorders (INR 1.5 or higher on the last blood coagulation test before surgery) - Patients with systemic infection - Patients with current infection in the area where dorsal transverse fascial block will be performed - Chronic pain patients - Patients who expressed their intention not to participate in this study - Patients allergic to local anesthetics - Patients with a serious psychiatric history that may affect patient evaluation

Design outcomes

Primary

MeasureTime frame
Opioid consumption during 24 hours postoperative

Secondary

MeasureTime frame
Opioid consumption;Pain score (representing by 11-points Numerous Rating Scale);Nausea, Vomiting, Pruritis, Respiratory depression;Delirium; Adverse event related procedure;socre of the questionaire of QoR-15 score before and after the surgery;satisfaction for analgesia;Satisfaction for sleep quality;ropivacaine plasma concentrations;first gas-out time

Countries

Korea, Republic of

Contacts

Public ContactYu Jeong Bang

Samsung Medical Center

gagreflex.bang@gmail.com+82-2-3410-2468

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026