Postoperative analgesic effect of transabdominis plane block patients undergoing open abdominal aortic surgery; a randomized controlled trial
- Conditions
- Diseases of the circulatory system
- Registration Number
- KCT0009160
- Lead Sponsor
- Samsung Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 86
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
- 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
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Opioid consumption during 24 hours postoperative
- Secondary Outcome Measures
Name Time Method 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