About this trial
This study aims to focus on patients undergoing gynecological laparoscopic surgery and further evaluate the role of amisulpride in preventing postoperative nausea and vomiting in these patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
1. 18<BMI≤30kg/m2 2. Patients scheduled to undergo gynecological laparoscopic surgery (e.g., ovary, fallopian tube, uterus, and gynecological tumors, etc., with an expected surgery duration of ≤3 hours)
Disqualifiers
1. ASA class IV or above 2. Long-term use of opioid drugs or non-steroidal anti-inflammatory drugs 3. Undergoing radiotherapy and chemotherapy 4.Allergic to the medication used 5.Pregnant or breastfeeding women 6.Previously existing vestibular disorders or chronic dizziness, easily nauseous 7.Recent use of antiemetic drugs or prophylactic antiemetic regimen (within 7 days before surgery) 8.Presence of neurological or psychiatric disorders, or cognitive impairment
Trial population
Agree and sign the informed consent form
Trial design
Cohort
Prospective
Treatments tested in this trial
Tropisetron
Drugand receive tropisetron (2mg) as a postoperative prophylactic antiemetic
Treatment groups
Trial outcomes
Primary outcomes
Complete remission (CR) rate within 24 hours postoperatively
The proportion of patients who, within 24 hours after surgery, experience neither vomiting episodes (vomiting/retching) nor require rescue antiemetic medication
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: