UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038087
Receipt number R000043407
Scientific Title Squatting test-1
Date of disclosure of the study information 2019/10/01
Last modified on 2019/09/24 10:18:17

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Basic information

Public title

Development and evaluation of a new method to determine the autonomic nervous system, and its application to perioperative management

Acronym

Development and evaluation of a new method to determine the autonomic nervous system, and its application to perioperative management

Scientific Title

Squatting test-1

Scientific Title:Acronym

Squatting test-1

Region

Japan


Condition

Condition

healthy volunteers

Classification by specialty

Anesthesiology Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of the study is to determine the optimal testing interval for the squatting test to determine cardiovagal baroreflex sensitivity in humans.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Correlation coefficients

Key secondary outcomes

Baroreflex sensitivities


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

65 years-old >

Gender

Male and Female

Key inclusion criteria

Healthy volunteers taking no medication.

Key exclusion criteria

Subjects with a history of cardiovascular, respiratory or metabolic disorders are excluded.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Makoto
Middle name
Last name Tanaka

Organization

University of Tsukuba, faculty of medicine

Division name

Department of Anesthesiology

Zip code

305-8575

Address

Tennoudai 1-1-1, Tsukuba-city, Ibaraki-ken

TEL

029-853-3285

Email

mtanaka@md.tsukuba.ac.jp


Public contact

Name of contact person

1st name Makoto
Middle name
Last name Tanaka

Organization

University of Tsukuba, faculty of medicine

Division name

Department of Anesthesiology

Zip code

305-8575

Address

Tennoudai 1-1-1, Tsukuba-city, Ibaraki-ken

TEL

029-853-3285

Homepage URL


Email

mtanaka@md.tsukuba.ac.jp


Sponsor or person

Institute

University of Tsukuba

Institute

Department

Personal name



Funding Source

Organization

Ministry of Education, Culture, Sports and Science

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tsukuba Clinical Research and Development Organization

Address

Amakuba 2-1-1, Tsukuba-city, Ubaraki-ken

Tel

029-853-3914

Email

igawa.junko.fu@un.tsukuba.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

筑波大学附属病院


Other administrative information

Date of disclosure of the study information

2019 Year 10 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

Preinitiation

Date of protocol fixation

2019 Year 09 Month 30 Day

Date of IRB

2019 Year 09 Month 18 Day

Anticipated trial start date

2019 Year 10 Month 01 Day

Last follow-up date

2019 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Baroreflex sensitivities were determined in duplicate by the squatting test at an interval of 30 s, 1 min and 3 min, and determine the correlation coefficients at each interval.


Management information

Registered date

2019 Year 09 Month 24 Day

Last modified on

2019 Year 09 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043407


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name