UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016977
Receipt number R000019704
Scientific Title Effectiveness of ramosetron in preventing post-operative nausea and vomiting: a systematic review and meta-analysis with trial sequential analysis
Date of disclosure of the study information 2015/04/01
Last modified on 2016/07/01 16:38:26

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Basic information

Public title

Effectiveness of ramosetron in preventing post-operative nausea and vomiting: a systematic review and meta-analysis with trial sequential analysis

Acronym

Effectiveness of ramosetron in preventing post-operative nausea and vomiting: a systematic review and meta-analysis with trial sequential analysis

Scientific Title

Effectiveness of ramosetron in preventing post-operative nausea and vomiting: a systematic review and meta-analysis with trial sequential analysis

Scientific Title:Acronym

Effectiveness of ramosetron in preventing post-operative nausea and vomiting: a systematic review and meta-analysis with trial sequential analysis

Region

Japan


Condition

Condition

Patients who underwent surgery with general anesthesia

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this meta-analysis was to update the evaluation of the effectiveness of ramosetron in preventing PONV

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The primary outcome from the present meta-analysis concerned PON and POV between ramosetron and ondansetron or a placebo in the early and/or late periods (defined later in this section).

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

all double-blinded randomized controlled trials that tested the efficacy of ramosetron compared with a placebo or other drug as a control in the prophylaxis of PONV

Key exclusion criteria

Studies which were reported by Fujii et al.
Studies which did not include details of PON and/or POV, or the early and/or late periods.
Data from case reports, comments or letters to the editor, reviews, and animal studies.

Target sample size



Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takahiro Mihara

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Anesthesiology and Critical Care Medicine

Zip code


Address

3-9 Fukuura, Kanazawa-ku, Yokohama 236-0004, Japan

TEL

045-787-2800

Email

miharaxxxtotoro@yahoo.co.jp


Public contact

Name of contact person

1st name
Middle name
Last name Takahiro Mihara

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Anesthesiology and Critical Care Medicine

Zip code


Address

3-9 Fukuura, Kanazawa-ku, Yokohama 236-0004, Japan

TEL

045-787-2800

Homepage URL


Email

miharaxxxtotoro@yahoo.co.jp


Sponsor or person

Institute

Yokohama City University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2015 Year 04 Month 01 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Terminated

Date of protocol fixation

2015 Year 03 Month 30 Day

Date of IRB


Anticipated trial start date

2015 Year 04 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

The study protocol was uploaded on this site. The file name is "prespecified protocol_ramosetroan".


Management information

Registered date

2015 Year 03 Month 30 Day

Last modified on

2016 Year 07 Month 01 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000019704