A Combined Thoracic Interfascial Plane Block for Postoperative Pain Relief and Quality of Recovery after Breast Cancer Surgery: A Prospective, Observational Cohort Study
Not Applicable
- Conditions
- Patients undergoing breast cancer surgery
- Registration Number
- JPRN-UMIN000039651
- Lead Sponsor
- Department of Anesthesia, Bell Land General Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who do not agree with this study, pregnant and parturient women, allergy to local anesthetics, significant psychiatric or mental disorders, patients with chronic pain.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analog Scale (VAS) pain score 3 hours after surgery
- Secondary Outcome Measures
Name Time Method Visual Analog Scale (VAS) pain score for "morning following surgery" and "maximum until the morning after surgery." Quality of Recovery (QoR-40; questionnaire consisting of 40 items) before and three days after surgery, 1, 3, 6, and 12 months after surgery. Patient age, height, weight, gender Surgery time Total fentanyl usage, total remifentanil usage Postoperative nausea and vomiting Frequent use of postoperative analgesics Time to need the first rescue analgesia Whether there are complications associated with the block (vascular puncture, pneumothorax, hematoma, nerve damage, etc.)