UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000022365
Receipt number R000023952
Scientific Title The survey of perioperative anaphylaxis in Gunma University Hospital and neighbor hospitals
Date of disclosure of the study information 2016/05/25
Last modified on 2020/05/22 15:08:59

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Basic information

Public title

The survey of perioperative anaphylaxis in Gunma University Hospital and neighbor hospitals

Acronym

The survey of perioperative anaphylaxis

Scientific Title

The survey of perioperative anaphylaxis in Gunma University Hospital and neighbor hospitals

Scientific Title:Acronym

The survey of perioperative anaphylaxis

Region

Japan


Condition

Condition

Perioperative anaphylaxis

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To survey the occurrences of drug-induced perioperative anaphylaxis in Gunma University Hospital and neighbor hospitals

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

To calculate the incidence rate of each drug-induced perioperative anaphylaxis

Key secondary outcomes

To analyze the risk factor of anaphylaxis during anesthesia


Base

Study type

Observational


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

110 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients who received anesthesia in the participating hospitals between January 1st, 2009 and December 31st, 2018

Key exclusion criteria

Patients who refused to participate to the study

Target sample size

180000


Research contact person

Name of lead principal investigator

1st name Tomonori
Middle name
Last name Takazawa

Organization

Gunma University Hospital

Division name

Department of Anesthesiology

Zip code

371-8511

Address

3-39-15 Showa-machi, Maebashi , Gunma, Japan 371-8511

TEL

0272208454

Email

takazawt@gunma-u.ac.jp


Public contact

Name of contact person

1st name Tomonori
Middle name
Last name Takazawa

Organization

Gunma University Hospital

Division name

Department of Anesthesiology

Zip code

371-8511

Address

3-39-15 Showa-machi, Maebashi , Gunma, Japan 371-8511

TEL

027-220-7111

Homepage URL


Email

takazawt@gunma-u.ac.jp


Sponsor or person

Institute

Gunma University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Gunma University

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

Gunma University Ethical Review Board for Medical Research Involving Human Subjects

Address

3-39-15 Showa-machi, Maebashi , Gunma, Japan 371-8511

Tel

027-220-7111

Email

hitotaisho-ciru@ml.gunma-u.ac.jp


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

伊勢崎市民病院(群馬県)、群馬県済生会前橋病院(群馬県)、足利赤十字病院(栃木県)、群馬中央病院(群馬県)、高崎総合医療センター(群馬県)、群馬県立心臓血管センター(群馬県)、群馬県立がんセンター(群馬県)、埼玉県立がんセンター(埼玉県)、桐生厚生総合病院(群馬県)、日高病院(群馬県)、高瀬クリニック(群馬県)、深谷赤十字病院(埼玉県)、渋川医療センター(群馬県)、利根中央病院(群馬県)、荻窪病院(東京都)、関東労災病院(神奈川県)、栃木県済生会宇都宮病院(栃木県)、自治医科大学(栃木県)、佐久医療センター(長野県)、四谷メディカルキューブ(東京都)


Other administrative information

Date of disclosure of the study information

2016 Year 05 Month 25 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

Enrolling by invitation

Date of protocol fixation

2016 Year 05 Month 12 Day

Date of IRB


Anticipated trial start date

2016 Year 05 Month 12 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

We will survey the incidence of anaphylaxis and the total amount of each agents used in operation room of participating hospitals


Management information

Registered date

2016 Year 05 Month 19 Day

Last modified on

2020 Year 05 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023952


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name