Single-center, randomized, parallel-group comparative study on efficacy and safety of preoperative peripheral nerve block-administered group and control group for human breast cancer with postoperative acute pain and persistent postoperative pai
Not Applicable
- Conditions
- Patients scheduled for breast cancer surgery
- Registration Number
- JPRN-UMIN000046644
- Lead Sponsor
- ational Defense Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
Underage, taking antipsychotics, psychiatric patients, severe obesity(>=BMI35), men, patients with chronic pain, patients taking opioids and analgesics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method