UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000014007
Receipt number R000016300
Scientific Title Non-invasive blood pressure monitoring using Doppler flow meter and ECG signals.
Date of disclosure of the study information 2014/05/20
Last modified on 2015/12/21 16:20:58

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Basic information

Public title

Non-invasive blood pressure monitoring using Doppler flow meter and ECG signals.

Acronym

Blood pressure monitoring with Doppler flow.

Scientific Title

Non-invasive blood pressure monitoring using Doppler flow meter and ECG signals.

Scientific Title:Acronym

Blood pressure monitoring with Doppler flow.

Region

Japan


Condition

Condition

Not specified

Classification by specialty

Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Development of monitoring apparatus for blood pressure using ECG and Doppler flow signals

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Acuity of blood pressure derived from the new apparatus.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Device,equipment

Interventions/Control_1

Recording of ECG, blood pressure and Doppler flow signals.

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

Male and Female

Key inclusion criteria

Patients under general anesthesia or staying in the ICU at the Kawasaki Medical Hospital.

Key exclusion criteria

Patients who did not agree to participate in the study.

Target sample size

100


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Yoshihisa Fujita

Organization

Kawasaki Medical School

Division name

Anesthesiology & ICM 1

Zip code


Address

577 Matsushima Kurashiki-City Okayama 701-0192

TEL

086-462-1111

Email

fujitay@med.kawasaki-m.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Yoshihisa Fujita

Organization

Kawasaki Medical School

Division name

Anesthesiology & ICM 1

Zip code


Address

577 Matsushima Kurashiki-City Okayama 701-0192

TEL

086-462-1111

Homepage URL


Email

fujitay@med.kawasaki-m.ac.jp


Sponsor or person

Institute

Kawasaki Medical School
Anesthesiology & ICM 1

Institute

Department

Personal name



Funding Source

Organization

Japan Society of the Promotion of Sciences. Grants-in-Aid for Scientific Research

Organization

Division

Category of Funding Organization

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

None

Name of secondary funder(s)

None


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

川崎医科大学附属病院(岡山県)


Other administrative information

Date of disclosure of the study information

2014 Year 05 Month 20 Day


Related information

URL releasing protocol


Publication of results

Partially published


Result

URL related to results and publications

http://www.asaabstracts.com/

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

Completed

Date of protocol fixation

2012 Year 04 Month 01 Day

Date of IRB


Anticipated trial start date

2014 Year 05 Month 20 Day

Last follow-up date

2015 Year 10 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2014 Year 05 Month 20 Day

Last modified on

2015 Year 12 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000016300


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name