Comparison of the effects of palonosetron and ramosetron mixed with intravenous patient-controlled analgesia infusion fluid
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0004834
- Lead Sponsor
- Inje University Haeundae Paik Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 114
Inclusion Criteria
1. Female patients aged 20-70
2. patients who underwent gynecologic laparoscopic surgery
3. patients receiving intravenous patient controlled analgesia after surgery
Exclusion Criteria
(1) ASA classification 3 or above,
(2) history of adverse events and hypersensitivity to serotonin receptor antagonists,
(3) refusal to participate in the study,
(4) obesity (body mass index over 30 kg/m2),
(5) refusal to undergo pain control through IV-PCA,
(6) pregnancy and lactation state.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method postoperative nausea incidence and severity
- Secondary Outcome Measures
Name Time Method postoperative pain severity