SUPplementary REgional anesthesia in MAmma surgery (SUPREMA trial).
Recruiting
- Conditions
- Mamma surgeryBreast cancerBorst operatieBorstkanker
- Registration Number
- NL-OMON22294
- Lead Sponsor
- .P.TanApotheek Reinier de Graaf Groep DelftPostbus 50112600 GA Delftvtan@rdgg.nlNo sponsors
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 150
Inclusion Criteria
1. Women;
2. One-sided breast conserving surgery with or without sentinel node biopsy;
Exclusion Criteria
1. Known allergy to amide type local anesthetics;
2. Severe liver failure;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative vomiting in the first 24 hours.
- Secondary Outcome Measures
Name Time Method 1. Postoperative nausea at entrance at entry in the recovery room and 4,8 and 24 hours after surgery (VAS score 0-10 cm);<br /> <br>2. Postoperative pain at entrance at entry in the recovery room and 4,8 and 24 hours after surgery (VAS score 0-10 cm);<br /> <br>3. Need for postoperative opiates (frequency and total dose in first 24 hours);<br /><br>4. Need for postoperative anti-emetics (frequency and total dose in first 24 hours).<br>