Postoperative Analgesic efficacy of continuous wound INfusion after laparoscopy (PAIN): a randomized, double-blind, placebo-controlled trial
Not Applicable
- Conditions
- Not Applicable
- Registration Number
- KCT0003439
- Lead Sponsor
- Kangbuk Samsung Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- 66
Inclusion Criteria
age between 18 and 65 years,
- American Society of Anesthesiologists physical status (ASAPS) classification I–II,
- absence of pregnancy at the time of surgery
Exclusion Criteria
- allergy to ropivacaine,
- laparoscopic surgery needing = 3 separate skin incisions,
- history of ventral or incisional hernia, pre-existing coagulopathy, neurologic or cognitive dysfunction,
- systemic or regional (especially, umbilicus) infection,
- previously taking opioids for chronic pain, or
- inability to accurately express their pain.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the severity of postoperative pain
- Secondary Outcome Measures
Name Time Method the degree of postoperative nausea and vomiting (PONV)