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Effect of Ramosetron on Post-discharge Nausea and Vomiting

Effect of Ramosetron on Post-discharge Nausea and Vomiting in Patients Undergoing Gynecologic Surgery Through a Day-surgery Center

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03409835
Enrollment
100
Registered
2018-01-24
Start date
2018-03-01
Completion date
2019-06-30
Last updated
2018-04-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hysteroscopy

Brief summary

Nausea and vomiting after general anesthesia is one of the common anesthetic complications. If the patient is discharged from the hospital after surgery, proper treatment may be delayed or impossible if nausea or vomiting occurs. Thus, It is necessary to prevent these symptoms beforehand. Patients who underwent gynecologic surgery will be treated with prophylactic ramosetron to determine whether the frequency of nausea and vomiting is decreased when the patient returned home after discharge.

Interventions

DRUGRamosetron

Ramosetron 0.3 mg is administered after induction of general anesthesia.

DRUGNormal saline

Normal saline 2 ml is administered after induction of general anesthesia.

Sponsors

Seoul National University Bundang Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patients who undergo hysteroscopic surgery and are discharged on the day of surgery.

Exclusion criteria

* American Society of Anesthesiologists physical statue 3 or more * Planned admission after surgery * Intravenous anesthesia * During chemotherapy * Pregnancy or breastfeeding * Abnormal liver or kidney function

Design outcomes

Primary

MeasureTime frame
The change in the occurrence of postoperative nauseaPostoperative 30 minute, 3 hour, 24 hour, and 48 hour
The change in the occurrence of postoperative vomitingPostoperative 30 minute, 3 hour, 24 hour, and 48 hour

Secondary

MeasureTime frameDescription
The change of postoperative pain scorePostoperative 30 minute, 3 hour, 24 hour, and 48 hourScore range is from 0 to 10.
The change in the number of postoperative administration of rescue analgesic drugPostoperative 30 minute and 3 hour
The change in the number of postoperative administration of rescue antiemetic drugPostoperative 30 minute and 3 hour
The change of patient's satisfaction scorePostoperative 30 minute, 3 hour, 24 hour, and 48 hourScore range is from 0 to 10.

Countries

South Korea

Contacts

Primary ContactHyo-Seok Na
hsknana@gmail.com1087012913

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026