The Effect of Oral and Intravenous Ramosetron During Laparoscopic Cholecystectomy
Not Applicable
- Conditions
- NauseaVomitingLaparoscopic Cholecystectomy
- Interventions
- Registration Number
- NCT01041183
- Lead Sponsor
- Seoul National University Bundang Hospital
- Brief Summary
Patients undergoing general anesthesia for laparoscopic cholecystectomy have a high risk of postoperative nausea and vomiting (PONV). The investigators investigated the effect of oral and IV ramosetron on PONV prophylaxis after laparoscopic cholecystectomy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
- ASA I-II patients, 25-65 years, electivelaparoscopic cholecystectomy under general anesthesia
Exclusion Criteria
- GI disease, pregnant or menstruating, history of motion sickness and/or postoperative emesis, antiemetics within 24 h before surgery
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description group I intravenous ramosetron 0.3 mg IV ramosetron group II oral ramosetron 0.1 mg oral ramosetron group III oral and IV ramosetron 0.1 mg oral ramosetron plus 0.3 mg IV ramosetron
- Primary Outcome Measures
Name Time Method Incidence of PONV postoperative 0-48 h
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Jung-Hee Ryu
🇰🇷Seongnam-si, Gyeonggi-do, Korea, Republic of