UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019182
Receipt number R000022151
Scientific Title The effects of fluctuation of central venous pressure on intraocular pressure
Date of disclosure of the study information 2015/09/30
Last modified on 2022/10/17 20:39:01

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Basic information

Public title

The effects of fluctuation of central venous pressure on intraocular pressure

Acronym

The effects of fluctuation of CVP on IOP

Scientific Title

The effects of fluctuation of central venous pressure on intraocular pressure

Scientific Title:Acronym

The effects of fluctuation of CVP on IOP

Region

Japan


Condition

Condition

single ventricle

Classification by specialty

Cardiology Pediatrics Cardiovascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To measure of IOP and CVP before and after the Fontan operation(including of the pulmonary artery banding and the Glenn operation)

Basic objectives2

Others

Basic objectives -Others

understanding of the disease

Trial characteristics_1

Exploratory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

IOP and CVP before and after the operations

Key secondary outcomes

sex
operative method
family history of glaucoma


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


Not applicable

Gender

Male and Female

Key inclusion criteria

Infants before the Fontan operation accepted this study

Key exclusion criteria

1 patients had glaucoma surgery
2 glaucoma patients
3 patients suspected development glaucoma
4 patients whom a study person in charge judged to be inappropriate as a study subject

Target sample size

10


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shinki Chin

Organization

Hokkaido University graduate school of medicine

Division name

ophthalmology

Zip code


Address

Kita 15, Nishi7, Kita-Ku, Sapporo, Hokkaido, Japan

TEL

011-706-5944

Email

schin@med.hokudai.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Riki Kijima

Organization

Hokkaido University graduate school of medicine

Division name

ophthalmology

Zip code


Address

Kita 15, Nishi7, Kita-Ku, Sapporo, Hokkaido, Japan

TEL

011-706-5944

Homepage URL


Email

riki-k@med.hokudai.ac.jp


Sponsor or person

Institute

Hokkaido University Hospital

Institute

Department

Personal name



Funding Source

Organization

none

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


Address


Tel


Email



Secondary IDs

Secondary IDs

YES

Study ID_1

015-0157

Org. issuing International ID_1

Hokkaido University Hospital Clinical Research and Medical Innovation Center

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 09 Month 30 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

no 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

2015 Year 09 Month 28 Day

Date of IRB

2015 Year 09 Month 30 Day

Anticipated trial start date

2015 Year 10 Month 01 Day

Last follow-up date

2020 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Prospective observational study
2015/9/30-2022/3/31(Registration deadline2017/3/31)
The patients before and after Fontan procedure and related procedures, those met the selection criteria.
We evaluate CVP, IOP, sex, operative procedures, and family history of glaucoma.


Management information

Registered date

2015 Year 09 Month 30 Day

Last modified on

2022 Year 10 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022151


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name