UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000045352
Receipt number R000051788
Scientific Title Comparison of Nasal pillow noninvasive positive pressure ventilation and high flow nasal therapy for the treatment and prevention of post extubation failure in intensive care patients
Date of disclosure of the study information 2021/09/02
Last modified on 2022/09/05 19:37:03

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Basic information

Public title

Comparison of Nasal pillow noninvasive positive pressure ventilation and high flow nasal therapy for the treatment and prevention of post extubation failure in intensive care patients

Acronym

Comparison of Nasal pillow noninvasive positive pressure ventilation and high flow nasal therapy for the treatment and prevention of post extubation failure in intensive care patients

Scientific Title

Comparison of Nasal pillow noninvasive positive pressure ventilation and high flow nasal therapy for the treatment and prevention of post extubation failure in intensive care patients

Scientific Title:Acronym

Comparison of Nasal pillow noninvasive positive pressure ventilation and high flow nasal therapy for the treatment and prevention of post extubation failure in intensive care patients

Region

Japan


Condition

Condition

ICU patients

Classification by specialty

Intensive care medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To prove the hypothesis that nasal pillow noninvasive positive pressure ventilation (NP-NPPV) has the same tolerability as high flow nasal therapy (HFNT) and higher respiratory support capacity than HFNT in patients after extubation

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The primary outcomes were respiratory parameters (PO2/FIO2 ratio, PCO2, respiratory rate) and tolerability of each interface immediately after extubation and 24 hours later.

Key secondary outcomes

The secondary outcomes were the duration of device use, the rate of device withdrawal after 24 hours, and the incidence of skin injury associated with the interface.


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who underwent NP-NPPV or HFNT after extubation to prevent post-extubation failure after more than 24 hours of ventilatory management after surgery

Key exclusion criteria

Non-operative patients, patients who did not require ventilatory management for more than 24 hours postoperatively, patients younger than 18 years, patients who used both NP-NPPV and HFNT, tracheostomy, head and neck surgery, significant neurological disorders, patients who used NPPV or HFNT preoperatively

Target sample size

100


Research contact person

Name of lead principal investigator

1st name Yoshifumi
Middle name
Last name Ohchi

Organization

Oita University

Division name

Department of Anesthesiology and Intensive Care, Faculty of Medicine

Zip code

879-5593

Address

1-1 Idaigaoka, Hasamamachi, Yufu City, Oita

TEL

0975865943

Email

ohchi-yo@oita-u.ac.jp


Public contact

Name of contact person

1st name Yoshifumi
Middle name
Last name Ohchi

Organization

Oita University

Division name

Department of Anesthesiology and Intensive Care, Faculty of Medicine

Zip code

879-5593

Address

1-1 Idaigaoka, Hasamamachi, Yufu City, Oita

TEL

0975865943

Homepage URL

http://anesth.wp.med.oita-u.ac.jp/research1/631

Email

ohchi-yo@oita-u.ac.jp


Sponsor or person

Institute

Department of Anesthesiology and Intensive Care, Faculty of Medicine, Oita University

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

Oita University Faculty of Medicine Ethics Committee

Address

1-1 Idaigaoka, Hasamamachi, Yufu City, Oita

Tel

097-586-6380

Email

rinrikenkyu@oita-u.ac.jp


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

大分大学医学部附属病院(大分県)


Other administrative information

Date of disclosure of the study information

2021 Year 09 Month 02 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications

https://journals.sagepub.com/doi/10.1177/03000605221112777?url_ver=Z39.88-2003&rfr_id=ori:rid:crossr

Number of participants that the trial has enrolled

110

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

2019 Year 09 Month 13 Day

Date of IRB

2019 Year 09 Month 13 Day

Anticipated trial start date

2019 Year 09 Month 13 Day

Last follow-up date

2021 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Under the analysis of the obtained data


Management information

Registered date

2021 Year 09 Month 02 Day

Last modified on

2022 Year 09 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051788


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name