The efficacy of pectoral nerve block for breast surgery
Not Applicable
Completed
- Conditions
- Neoplasms
- Registration Number
- KCT0002509
- Lead Sponsor
- Asan Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
1) The patients with early breast cancer who would undergo breast conserving surgery and sentinel lymph node biopsy
2) All patients were from 20 years to 70 years
3) ASA physical status I and II
4) The patients who voluntarily agree with this clinical trial
Exclusion Criteria
1) allergies to local anesthetics
2) anticoagulation use
3) serious neurological or psychiatric disorders
4) no co-operability
5) pregnancy and breastfeeding
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the difference of postoperative opioid consumption between two groups during 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method Postoperative pain intensity at 0, 1/2, 1, 2, 6, 9, 18, 24 hours after end of surgery;Opioid requirements according to breast cancer location;Side effects of analgesics;Complications of the PECS II block