Palonosetron for day care gynaecological procedures

Comparison of different doses of palonosetron for postoperative nausea vomiting in patients undergoing day care laparoscopic gynecological procedures- A Randomized controlled Trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2014/09/004987

Enrollment

120

Registered

2014-09-08

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Palonosetron 1mcg/kg: Palonosetron 1mcg/kg given before induction of anaesthesia Intervention2: Palonosetron 1mcg/kg: Palonosetron 1mcg/kg given before induction of anaesthesia Control

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I or II age group of 18-60 years undergoing laparoscopic gynaecological procedures on day care basis

Exclusion criteria

Exclusion criteria: Patients allergic to 5HT3 receptor antagonist , history of gastrointestinal diseases,history of motion sickness ,history of postoperative nausea vomiting , having body mass index >30 or if the surgical procedure was converted to laparotomy

Design outcomes

Primary

Measure	Time frame
complete response during for the first 72Timepoint: complete response during for the first 72	—

Secondary

Measure	Time frame
Postoperative nausea vomitingTimepoint: 2,6,12,24,48,72 hrs	—

Countries

India

Contacts

Public ContactDivya Jain

PGIMER

jaindivya77@rediffmail.com91-9855900171

Outcome results