Evaluation of ultrasound-guided rhomboid intercostal nerve block for postoperative analgesia in breast cancer surgery: A prospective, randomized, controlled trial
Not Applicable
Completed
- Conditions
- breast cancerpostoperative painCancer - BreastAnaesthesiology - Pain management
- Registration Number
- ACTRN12619000879167
- Lead Sponsor
- Basak ALTIPARMAK
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Patients between 18-70 years old, with American Society of Anesthesiologists (ASA) physical status I-II, and scheduled for an elective unilateral mastectomy surgery with sentinel node biopsy and Modified Radical Mastectomy surgery with axillary lymph node dissection.
Exclusion Criteria
Patients with coagulation disorder, chronic opioid use, psychologic disorder, known allergy to study drugs, history of previous mastectomy or other thoracic surgery, body mass index >? 35 kg m2, inability to use patient-controlled analgesia (PCA) device and surgical time longer than 150 minutes.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method quality of recovery levels between groups by using 40-point QoR-40 questionnaire[At the postoperative 24th hour ]
- Secondary Outcome Measures
Name Time Method Postoperative pain scores between groups by using 11-points Numerical Rating Scale scores [At the postoperative 15th min and 30th min, 1st h (secondary time-point), 2nd h, 6th h, 12th h, and 24th h];rescue analgesic consumptions between groups as assessed by data linkage to medical records [at the postoperative 24th hour ];Total postoperative morphine consumption in the first 24 hour. Morphine consumption will be calculated directly checking the morphine delivery times recorded on patient-controlled-analgesia devise.[At the postoperative 24th hour ]