FindTrial
Sign In

The optimize rescue strategy after the failure of the prevention of the postoperative nausea and vomiting

The optimize rescue strategy after the failure of the prevention of the postoperative nausea and vomiting

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009763
Enrollment
Unknown
Registered
2016-11-06
Start date
2016-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

postoperative nausea and vomiting

Interventions

Droperidol group:Droperidol 0.625mg
Metoclopramide group:Metoclopramide 10mg
Propofol group:Propofol 20mg

Sponsors

Anesthesia Department of the Second Affiliated Hospital of the Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: After general anesthesia using drugs for the prevention of postoperative nausea and vomiting, the incidence of postoperative nausea and vomiting still excited patients aged 18 to 60 years, ASA I or II.

Exclusion criteria

Exclusion criteria: 1. allergy to the medicine; 2. disaggree to participate in the trial.

Design outcomes

Primary

MeasureTime frame
visual analogue scale of nausea and vomiting ;—

Countries

China

Contacts

Public ContactZHANG BING

Anesthesia Department of the Second Affiliated Hospital of the Harbin Medical University

zhang_bing08@126.com+86 13796620602

Outcome results

None listed

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