UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000027480
Receipt number R000031426
Scientific Title Plasma concentration of vascular endothelial growth factor in very low birth weight infants at Nagaoka Red Cross hospital
Date of disclosure of the study information 2017/05/25
Last modified on 2017/05/23 23:35:49

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Basic information

Public title

Plasma concentration of vascular endothelial growth factor in very low birth weight infants at Nagaoka Red Cross hospital

Acronym

Plasma concentration of vascular endothelial growth factor in very low birth weight infants at Nagaoka Red Cross hospital

Scientific Title

Plasma concentration of vascular endothelial growth factor in very low birth weight infants at Nagaoka Red Cross hospital

Scientific Title:Acronym

Plasma concentration of vascular endothelial growth factor in very low birth weight infants at Nagaoka Red Cross hospital

Region

Japan


Condition

Condition

retinopathy of prematurity

Classification by specialty

Ophthalmology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To investigate the relationship between vascular endothelial growth factor (VEGF) and ROP by measuring plasma concentration of VEGF in very low birth weight infants at Nagaoka Red Cross hospital.

Basic objectives2

Others

Basic objectives -Others

To investigate the relationship between vascular endothelial growth factor (VEGF) and ROP by measuring plasma concentration of VEGF in very low birth weight infants at Nagaoka Red Cross hospital.

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

plasma concentration of VEGF

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

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Maneuver

Interventions/Control_1

200 micro litter blood collection every two week

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

very low birth weight infants

Key exclusion criteria

1.Infants that has too severe complications to collect blood samples
2.Infants whom parents decline to collect blood samples
3.Infants that invetigator assess not appropriate

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Hideaki Yoshino

Organization

Nagaoka Red Cross Hospital

Division name

Ophthalmology

Zip code


Address

Senshu-2 297-1, Nagaoka-shi, Niigata-ken, Japan

TEL

0258-28-3600

Email

ysnhoph@med.niigata-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Hideaki Yoshino

Organization

Nagaoka Red Cross Hospital

Division name

Ophthalmology

Zip code


Address

Senshu-2 297-1, Nagaoka-shi, Niigata-ken, Japan

TEL

0258-28-3600

Homepage URL


Email

ysnhoph@med.niigata-u.ac.jp


Sponsor or person

Institute

Nagaoka Red Cross Hospital

Institute

Department

Personal name



Funding Source

Organization

Niigata university medical and dental hospital

Organization

Division

Category of Funding Organization

Other

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

2639

Org. issuing International ID_1

Research Ethics Committee, niigata univercity

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2017 Year 05 Month 25 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

2016 Year 12 Month 06 Day

Date of IRB


Anticipated trial start date

2016 Year 12 Month 06 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

2017 Year 05 Month 24 Day

Last modified on

2017 Year 05 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031426


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name