UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038127
Receipt number R000043455
Scientific Title Development of a new sleep apnea diagnostic method using intravenous sedation
Date of disclosure of the study information 2019/10/01
Last modified on 2021/09/28 09:10:46

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Basic information

Public title

Development of a new sleep apnea diagnostic method using intravenous sedation

Acronym

Development of a new sleep apnea diagnostic method using intravenous sedation

Scientific Title

Development of a new sleep apnea diagnostic method using intravenous sedation

Scientific Title:Acronym

Development of a new sleep apnea diagnostic method using intravenous sedation

Region

Japan


Condition

Condition

intravenous sedation

Classification by specialty

Anesthesiology Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

During the management of intravenous sedation, upper airway obstruction is likely to occur, and this pathology is similar to the mechanism of maintaining upper airway patency during sleep, applying a new sleep apnea upper airway patency The aim is to develop a diagnosis of.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

upper airway patency

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Diagnosis

Type of intervention

Medicine

Interventions/Control_1

propofol

Interventions/Control_2

dexmedetomidine

Interventions/Control_3

ketamine

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

Healthy adult subjects who agreed to the study

Key exclusion criteria

Patients with serious systemic complications

Target sample size

40


Research contact person

Name of lead principal investigator

1st name TAKAO
Middle name
Last name AYUSE

Organization

Nagasaki University

Division name

Dental Anesthesia

Zip code

8528588

Address

1-7-1 Sakamoto Nagasaki

TEL

0958197713

Email

ayuse@nagasaki-u.ac.jp


Public contact

Name of contact person

1st name TAKAO
Middle name
Last name AYUSE

Organization

Nagasaki University Hospital

Division name

Dental Anesthesia

Zip code

8528588

Address

1-7-1 Sakamoto Nagasaki

TEL

0958197713

Homepage URL


Email

ayuse@nagasaki-u.ac.jp


Sponsor or person

Institute

Nagasaki University

Institute

Department

Personal name



Funding Source

Organization

Nagasaki University

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

Nagasaki University

Address

1-7-1 Sakamto

Tel

0958197198

Email

t-nakao@nagasaki-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

2019 Year 10 Month 01 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

2019 Year 04 Month 11 Day

Date of IRB

2019 Year 04 Month 11 Day

Anticipated trial start date

2019 Year 10 Month 01 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry

2023 Year 04 Month 30 Day

Date trial data considered complete

2023 Year 05 Month 31 Day

Date analysis concluded

2023 Year 06 Month 30 Day


Other

Other related information



Management information

Registered date

2019 Year 09 Month 27 Day

Last modified on

2021 Year 09 Month 28 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043455


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name