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Effect of palonosetron on postoperative nausea and vomiting (comparison with ondansetron and ramosetron)

Effect of palonosetron on patient-controlled analgesia related nausea and vomiting after thyroidectomy (comparison with ondansetron and ramosetron)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0000012
Enrollment
150
Registered
2010-07-05
Start date
2010-04-26
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Drug : Palonosetron: 0.075 mg intravenous injection 30 minutes ago completion of surgery

Sponsors

The Catholic University of Korea, Seoul St. Mary's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients undergoing thyroid surgery, with a risk of PONV exceeding 60% are selected according to the expected risk for PONV using the simplified risk score of Apfel et al. The 4 risk factors considered in this score are female gender, nonsmoking, the use of postoperative opioids, and prior history of motion sickness or PONV; the presence of 0, 1, 2, 3, or 4 of these risk factors correspond to approximately 10, 20, 40, 60, and 80% risk for PONV, respectively. Basic inclusion criteria are nonsmoking, female patients, and use of postoperative opioid.

Exclusion criteria

Exclusion criteria: Patients who have severe impairment of bowel motility, insulin-dependent diabetes mellitus, pregnancy or breastfeeding, administration of antiemetic medication within 24 hours before surgery, systemic treatment with steroids within 24 hours before surgery or during 48 hours after surgery, obesity (body mass index >=35 kg/m2),impaired renal and/or hepatic function, or require radical neck dissection

Design outcomes

Primary

MeasureTime frame
incidence and severity of postoperative nausea and vomiting

Secondary

MeasureTime frame
requirement for anti-emetic rescue medication ;pain degree (Visual analogue scale) and requirement for analgesic rescue medication;total dose of fentanyl used in intravenous patient-controlled analgesia;Incidence of side effects (Headache, dizziness, and drowsiness)

Countries

Korea, Republic of

Contacts

Public ContactYoung Eun Moon

The Catholic University of Korea, Seoul St. Mary's Hospital

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026