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SubstanceP and postoperative nausea and vimiting

SubstanceP and postoperative nausea and vimiting - SubstanceP and postoperative nausea and vimiting

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015318
Enrollment
30
Registered
2014-10-02
Start date
2014-04-07
Completion date
Unknown
Last updated
2026-06-29

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

We measured plasma levels of substanceP on the day before operation, intraoperative pediod and postoperative period.

Sponsors

Department of Anesthesiology, Tokushima University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Eligible patients meet the criteria of American Society of Anesthesiologists(ASA)physical status of I-II.

Exclusion criteria

Exclusion criteria: Patients are excluded the criteria of American Society of Anesthesiologists(ASA)physical status of over III.

Design outcomes

Primary

MeasureTime frame
Episodes of nausea and vomiting

Countries

Japan

Contacts

Public ContactNami Kakuta

Tokushima University Hospital Anesthesiology

kakuta.nami@tokushima-u.ac.jp088-633-7181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026