UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000042085
Receipt number R000048029
Scientific Title The examination of sedation depth of remimazolam in general anesthesia: Pilot study
Date of disclosure of the study information 2020/10/20
Last modified on 2022/04/14 10:01:18

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Basic information

Public title

The examination of sedation depth of remimazolam in general anesthesia: Pilot study

Acronym

The examination of sedation depth of remimazolam in general anesthesia: Pilot study

Scientific Title

The examination of sedation depth of remimazolam in general anesthesia: Pilot study

Scientific Title:Acronym

The examination of sedation depth of remimazolam in general anesthesia: Pilot study

Region

Japan


Condition

Condition

the patients of breast tumor

Classification by specialty

Breast surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To examine the objective evaluation of the depth of anesthesia of remimazolam, using by portable infrared pupilometer and BIS monitor.

Basic objectives2

Others

Basic objectives -Others

An objective assessment of the depth of anesthesia with remimazolam will be examined in terms of the degree of sympathetic excitation.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Relationship between BIS Values and Pupil Response

Key secondary outcomes

Relationship between Intraoperative EEG Monitored Values and Pupil Response


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

20 years-old <

Age-upper limit


Not applicable

Gender

Female

Key inclusion criteria

Patients undergoing breast surgery under general anesthesia.

Key exclusion criteria

Patients who are deemed by the investigator to be unsuitable as research subjects
(Underage, insufficient data.)

Target sample size

30


Research contact person

Name of lead principal investigator

1st name kazuhiro
Middle name
Last name shirozu

Organization

kyushu university hospital

Division name

anesthesia

Zip code

812-8582

Address

Maidashi 3-1-1, Higashi-ku, Fukuoka

TEL

092-642-5714

Email

shirozu.kazuhiro.334@m.kyushu-u.ac.jp


Public contact

Name of contact person

1st name kazuhiro
Middle name
Last name shirozu

Organization

kyushu university hospital

Division name

anesthesia

Zip code

812-8582

Address

Maidashi 3-1-1, Higashi-ku, Fukuoka

TEL

092-642-5714

Homepage URL


Email

shirozu.kazuhiro.334@m.kyushu-u.ac.jp


Sponsor or person

Institute

kyushu university hospital

Institute

Department

Personal name



Funding Source

Organization

kyushu university hospital

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

kyushu university hospital

Address

Maidashi 3-1-1, Higashi-ku, Fukuoka

Tel

092-642-6254

Email

ijkseimei@jimu.kyushu-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



Other administrative information

Date of disclosure of the study information

2020 Year 10 Month 20 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled

40

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

Completed

Date of protocol fixation

2020 Year 10 Month 05 Day

Date of IRB

2020 Year 10 Month 05 Day

Anticipated trial start date

2020 Year 10 Month 29 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2022 Year 03 Month 31 Day


Other

Other related information

prospective observational study


Management information

Registered date

2020 Year 10 Month 12 Day

Last modified on

2022 Year 04 Month 14 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048029


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name