UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018983
Receipt number R000021932
Scientific Title Effective and safe use of heated humified high flow nasal cannula in neonates.
Date of disclosure of the study information 2015/09/28
Last modified on 2016/03/23 19:22:53

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Basic information

Public title

Effective and safe use of heated humified high flow nasal cannula in neonates.

Acronym

Effective and safe use of heated humified high flow nasal cannula in neonates.

Scientific Title

Effective and safe use of heated humified high flow nasal cannula in neonates.

Scientific Title:Acronym

Effective and safe use of heated humified high flow nasal cannula in neonates.

Region

Japan


Condition

Condition

neonatal respiratory disorders

Classification by specialty

Pediatrics

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare the efficacy and safety between High-Flow Nasal Cannula and Nasal CPAP in infants with neonatal respiratory disorders over 28 gestational weeks.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Improvement rate of respiratory acidosis and hypercapnia 1 hour after intervention.

Key secondary outcomes

Improvement rate of oxygenation 1 hour after intervention.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

High-Flow Nasal Cannula group

Interventions/Control_2

Nasal CPAP group

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

28 weeks-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

- infants over 28 gestational weeks and birth weight over 1000g
- infants with neonatal respiratory disorder, who does not respond to initial nasal CPAP therapy
- infants who do not have indication of intubation

Key exclusion criteria

- infants intubated at hospitalization
- infants with nasal, oral or airway anomaly
- infants with air leak at hospitalization

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Atsuko Taki

Organization

Tokyo Medical and Dental University

Division name

Pediatrics

Zip code


Address

1-5-45 Yushima Bunkyo Tokyo

TEL

03-3813-6111

Email

ataki.ped@tmd.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Ryo AOKI

Organization

Tokyo Medical and Dental University

Division name

Pediatrics

Zip code


Address

1-5-45 Yushima Bunkyo Tokyo

TEL

03-3813-6111

Homepage URL


Email

ronron81818@gmail.com


Sponsor or person

Institute

Tokyo Medical and Dental University
Department of Pediatrics

Institute

Department

Personal name



Funding Source

Organization

None

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

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 09 Month 28 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

2015 Year 09 Month 28 Day

Date of IRB


Anticipated trial start date

2015 Year 11 Month 01 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 09 Month 11 Day

Last modified on

2016 Year 03 Month 23 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000021932


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name