UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000028137
Receipt number R000031021
Scientific Title Randomized controlled trial examining the effect of continuous positive airway pressure on arterial blood gases during one-lung ventilation
Date of disclosure of the study information 2017/07/07
Last modified on 2023/07/05 11:56:39

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Basic information

Public title

Randomized controlled trial examining the effect of continuous positive airway pressure on arterial blood gases during one-lung ventilation

Acronym

Effects of continuous positive airway pressure on arterial blood gases during one-lung ventilation

Scientific Title

Randomized controlled trial examining the effect of continuous positive airway pressure on arterial blood gases during one-lung ventilation

Scientific Title:Acronym

Effects of continuous positive airway pressure on arterial blood gases during one-lung ventilation

Region

Japan


Condition

Condition

Lung cancer,cystic lung disease

Classification by specialty

Chest surgery

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To measure changes in blood oxygen partial pressure for changing of administration oxygen concentration 60% or 100% of CPAP during the one lung.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

blood oxygen partial pressure at 30 minutes after the start of CPAP

Key secondary outcomes

Changes of blood oxygen partial pressure during 30 minutes after the start of CPAP


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Dose comparison

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

administration of oxygen concentration of CPAP 0% during one lung ventilation

Interventions/Control_2

administration of oxygen concentration of CPAP 100% during one lung ventilation

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

90 years-old >

Gender

Male and Female

Key inclusion criteria

Patients who require thoracic survey with one lung ventilation

Key exclusion criteria

History of ischemic heart disease and heart failure.
History of ischemic brain disease.
Interstitial pneumonia
SPO2 is less than 94%.
PaO2 is less than 70mmHg.
BMIis greater than 30 kg/m2.
ASA-PS classificationis greater than 3.

Target sample size

70


Research contact person

Name of lead principal investigator

1st name Yuko
Middle name
Last name Yamada

Organization

Gifu University Graduate School of Medicine

Division name

Anesthesiology and Pain Medicine

Zip code

5011194

Address

1-1 Yanagido, Gifu City, Gifu

TEL

058-230-6404

Email

y-comet@wg7.so-net.ne.jp


Public contact

Name of contact person

1st name Yuko
Middle name
Last name amada

Organization

Gifu University Graduate School of Medicine

Division name

Anesthesiology and Pain Medicine

Zip code

5011194

Address

1-1 Yanagido, Gifu City, Gifu

TEL

058-230-6404

Homepage URL


Email

y-comet@wg7.so-net.ne.jp


Sponsor or person

Institute

Gifu University Graduate School of Medicine

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

Gifu University Graduate School of Medicine

Address

1-1 Yanagido, Gifu City, Gifu

Tel

058-230-6404

Email

gjme00043@jim.gifu-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



Other administrative information

Date of disclosure of the study information

2017 Year 07 Month 07 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

70

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

2017 Year 07 Month 07 Day

Date of IRB

2016 Year 11 Month 17 Day

Anticipated trial start date

2017 Year 07 Month 07 Day

Last follow-up date

2027 Year 07 Month 07 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2017 Year 07 Month 07 Day

Last modified on

2023 Year 07 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000031021


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name