UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016295
Receipt number R000018905
Scientific Title Vasopressin V1a receptors and oxygen deficit at the start of voluntary locomotion
Date of disclosure of the study information 2015/01/21
Last modified on 2015/01/21 15:05:22

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Basic information

Public title

Vasopressin V1a receptors and oxygen deficit at the start of voluntary locomotion

Acronym

Voluntary locomotion and V1a receptors

Scientific Title

Vasopressin V1a receptors and oxygen deficit at the start of voluntary locomotion

Scientific Title:Acronym

Voluntary locomotion and V1a receptors

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To identify the role of vasopressin V1a receptors in pressor responses at the start of voluntary locomotion

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Pressor responses at the start of voluntary locomotion

Key secondary outcomes



Base

Study type


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit


Blinding

Single blind -investigator(s) and assessor(s) are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Nose drops of desmopressin

Interventions/Control_2

Nose drops of saline

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

70 years-old >=

Gender

Male

Key inclusion criteria

1) Healthy male adults
2) Those who want to participate in the study
3) Those who suffer minimum risks for their health wjen they participate in the study

Key exclusion criteria

1) Those who may suffer not negligible risks when they participate in the study

Target sample size

30


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hiroshi Nose

Organization

Shinshu University Graduate School of Medicine

Division name

Department of Sports Medical Sciences,

Zip code


Address

3-1-1 Asahi, Matsumoto

TEL

0263-37-2681

Email

nosehir@shinshu-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Naomi Ishikura

Organization

Shinshu University

Division name

School of Medicine

Zip code


Address

3-1-1 Asahi, Matsumoto

TEL

0263-37-2572

Homepage URL


Email

ishikura_naomi@gm.shinshu-u.ac.jp


Sponsor or person

Institute

Shinshu University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

MEXT

Organization

Division

Category of Funding Organization

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 01 Month 21 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

2015 Year 01 Month 21 Day

Date of IRB


Anticipated trial start date

2015 Year 01 Month 21 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 01 Month 21 Day

Last modified on

2015 Year 01 Month 21 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018905


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name