UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000043454
Receipt number R000049625
Scientific Title Study of intravenous sedation for elderly patients with severe dementia during dental treatment-comparison with healthy subjects by EEG analysis
Date of disclosure of the study information 2021/03/01
Last modified on 2021/08/02 20:01:02

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Basic information

Public title

Study of intravenous sedation for elderly patients with severe dementia during dental treatment-comparison with healthy subjects by EEG analysis

Acronym

Study of intravenous sedation for elderly patients with severe dementia

Scientific Title

Study of intravenous sedation for elderly patients with severe dementia during dental treatment-comparison with healthy subjects by EEG analysis

Scientific Title:Acronym

Study of intravenous sedation for elderly patients with severe dementia

Region

Japan


Condition

Condition

dementia

Classification by specialty

Neurology Anesthesiology Oral surgery
Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

In the intravenous sedation using midazolam during dental treatment, the intraoperative cerebral blood flow and EEG are measured and compared with between elderly patients with/ without cognitive impairment.

Basic objectives2

Others

Basic objectives -Others

The postoperative cognitive and swallowing declines are evaluated in the elderly patients with severe dementia.

Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

encephalography; measurement during midazolam administration

Key secondary outcomes

cerebral blood flow; measurement during midazolam administration


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Medicine

Interventions/Control_1

Intravenous sedation with midazolam for the elderly patients with severe dementia

Interventions/Control_2

Intravenous sedation with midazolam for the elderly patients without cognitive impairment

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

60 years-old <=

Age-upper limit

100 years-old >=

Gender

Male and Female

Key inclusion criteria

The elderly patients with severe dementia

Key exclusion criteria

The elderly patients without cognitive impairment
The patients who could not use midazolam for allergy or narrow-angle glaucoma

Target sample size

20


Research contact person

Name of lead principal investigator

1st name Yoshinari
Middle name
Last name Morimoto

Organization

Kanagawa Dental University

Division name

Division of Geriatric Dentistry, Department of Critical Care Dentistry

Zip code

238-8580

Address

82, Inaoka-cho, Yokosuka, Kanagawa, 238-8580, Japan

TEL

046-845-3168

Email

morimoto@kdu.ac.jp


Public contact

Name of contact person

1st name Yoshinari
Middle name
Last name Morimoto

Organization

Kanagawa Dental University

Division name

Division of Geriatric Dentistry, Department of Critical Care Dentistry

Zip code

238-8580

Address

82, Inaoka-cho, Yokosuka, Kanagawa, 238-8580, Japan

TEL

046-845-3168

Homepage URL


Email

morimoto@kdu.ac.jp


Sponsor or person

Institute

Division of Geriatric Dentistry, Department of Critical Care Dentistry, Kanagawa Dental University

Institute

Department

Personal name



Funding Source

Organization

Japan Society for the Promotion of Science (JSPS)

Organization

Division

Category of Funding Organization

Government offices of other countries

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kanagawa Dental University

Address

82, Inaoka-cho, Yokosuka, Kanagawa, 238-8580, Japan

Tel

046-845-3168

Email

morimoto@kdu.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

神奈川歯科大学附属病院


Other administrative information

Date of disclosure of the study information

2021 Year 03 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

2021 Year 03 Month 01 Day

Date of IRB

2021 Year 02 Month 25 Day

Anticipated trial start date

2021 Year 03 Month 08 Day

Last follow-up date

2025 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2021 Year 02 Month 27 Day

Last modified on

2021 Year 08 Month 02 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000049625


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name