UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000042557
Receipt number R000048575
Scientific Title The Impact of Surgical Masks on Oxygen Therapy with Oxygen Masks
Date of disclosure of the study information 2020/11/26
Last modified on 2022/06/20 23:47:57

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Basic information

Public title

The Impact of Surgical Masks on Oxygen Therapy with Oxygen Masks

Acronym

The Impact of Surgical Masks on Oxygen Therapy with Oxygen Masks

Scientific Title

The Impact of Surgical Masks on Oxygen Therapy with Oxygen Masks

Scientific Title:Acronym

The Impact of Surgical Masks on Oxygen Therapy with Oxygen Masks

Region

Japan


Condition

Condition

Adult Healthy Volunteers

Classification by specialty

Anesthesiology Intensive care medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Examine whether a surgical mask under an oxygen mask will affect oxygen therapy

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The fraction of inspired oxygen (FiO2) , The partial pressure of inspired carbon dioxide

Key secondary outcomes

The fraction of exhaled oxygen, The partial pressure of exhaled carbon dioxide, Percutaneous arterial oxygen saturation(SpO2)


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Device,equipment

Interventions/Control_1

Wearing an oxygen mask with a surgical mask

Interventions/Control_2

Wearing an oxygen mask without a surgical mask

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


Not applicable

Gender

Male and Female

Key inclusion criteria

Male and female adult volunteers aged 20 years or older with ASA(American Society of Anesthesia) PS(Physical Status) 1-2 with no underlying respiratory diseases and Hugh-Jones classification grade I

Key exclusion criteria

ASA PS3 or higher
Underlying respiratory disease and a Hugh-Jones classification of grade II or higher

Target sample size

15


Research contact person

Name of lead principal investigator

1st name Michiko
Middle name
Last name Kinoshita

Organization

Tokushima University Hospital

Division name

Anesthesiology

Zip code

770-8503

Address

2-50-1, Kuramoto-cho, Tokushima, Tokushima, Japan

TEL

088-633-7181

Email

michiko-kinoshita@tokushima-u.ac.jp


Public contact

Name of contact person

1st name Michiko
Middle name
Last name Kinoshita

Organization

Tokushima University Hospital

Division name

Anesthesiology

Zip code

770-8503

Address

2-50-1, Kuramoto-cho, Tokushima, Tokushima, Japan

TEL

088-633-7181

Homepage URL


Email

michiko-kinoshita@tokushima-u.ac.jp


Sponsor or person

Institute

Tokushima University Hospital, Anesthesiology

Institute

Department

Personal name



Funding Source

Organization

Tokushima University Hospital, Anesthesiology

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

The Ethics Committee of Tokushima University Hospital

Address

2-50-1, Kuramoto-cho, Tokushima, Tokushima, Japan

Tel

088-633-7181

Email

michiko-kinoshita@tokushima-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

2020 Year 11 Month 26 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled

15

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

2020 Year 11 Month 01 Day

Date of IRB

2020 Year 11 Month 09 Day

Anticipated trial start date

2020 Year 11 Month 26 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2020 Year 11 Month 26 Day

Last modified on

2022 Year 06 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048575


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name