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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	JPRN
Last refreshed on:	17 October 2023
Main ID:	JPRN-UMIN000015318
Date of registration:	02/10/2014
Prospective Registration:	No
Primary sponsor:	Department of Anesthesiology, Tokushima University Hospital
Public title:	SubstanceP and postoperative nausea and vimiting
Scientific title:	SubstanceP and postoperative nausea and vimiting - SubstanceP and postoperative nausea and vimiting
Date of first enrolment:	2014/04/07
Target sample size:	30
Recruitment status:	Complete: follow-up complete
URL:	https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016903
Study type:	Interventional
Study design:	Single arm Non-randomized
Phase:	Not selected

Countries of recruitment
Japan

Contacts

Name:	Nami Kakuta
Address:	Kuramoto 3-18-15, Tokushima 770-8503, Japan Japan
Telephone:	088-633-7181
Email:	kakuta.nami@tokushima-u.ac.jp
Affiliation:	Tokushima University Hospital Anesthesiology

Name:	Yasuo Tsutsumi
Address:	Kuramoto 3-18-15, Tokushima 770-8503, Japan Japan
Telephone:	088-633-7181
Email:	tsutsumi@tokushima-u.ac.jp
Affiliation:	Tokushima University Hospital Anesthesiology

Key inclusion & exclusion criteria

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

Age minimum: 20years-old
Age maximum: 80years-old
Gender: Male and Female

Health Condition(s) or Problem(s) studied

postoperative nausea and vomiting

Intervention(s)

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

Primary Outcome(s)

Episodes of nausea and vomiting

Secondary Outcome(s)

Secondary ID(s)

Source(s) of Monetary Support

Tokushima University Hospital

Secondary Sponsor(s)

Ethics review

Status: YES
Approval date:
Contact:

Results

Results available:
Date Posted:
Date Completed:
URL:

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