UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000006262
Receipt number R000007412
Scientific Title A research on complications and recovery time regarding to an ambulatory general anesthesia and an intravenous sedation for dental treatments on patients with intellectual disability.
Date of disclosure of the study information 2011/09/01
Last modified on 2015/07/17 20:13:12

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Basic information

Public title

A research on complications and recovery time regarding to an ambulatory general anesthesia and an intravenous sedation for dental treatments on patients with intellectual disability.

Acronym

A research on complications and recovery time regarding to an ambulatory general anesthesia and an intravenous sedation for dental treatments on patients with intellectual disability.

Scientific Title

A research on complications and recovery time regarding to an ambulatory general anesthesia and an intravenous sedation for dental treatments on patients with intellectual disability.

Scientific Title:Acronym

A research on complications and recovery time regarding to an ambulatory general anesthesia and an intravenous sedation for dental treatments on patients with intellectual disability.

Region

Japan


Condition

Condition

Intellectual disability

Classification by specialty

Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Objectives are patients with intellectual disability for whom ambulatory general anesthesia or intravenous sedation are planned. A purpose is to analyze relationship between various factors and complications as a cohort study.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Background of patient: Age, gender, height, weight, cerebral palsy, autism, epilepsy, medicines of dairy use.
Anesthetic data: induction method, amount of midazolam, administration speed of propofol, recovery time.
Treatment data: treatment time, kinds of dental treatment

Key secondary outcomes



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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Objectives are patients with intellectual disability for whom ambulatory general anesthesia or intravenous sedation are planned from December 1st 2009 to March 31st 2012.

Key exclusion criteria

Patients without intellectual disability.

Target sample size

600


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takuya Miyawaki

Organization

Okayama University Graduate School of Medicine, Dentistry and Parmaceutical Sciences

Division name

Department of Dental Anesthesiology and Special Care Dentistry

Zip code


Address

2-5-1 Shikata-cho, Kita-ku, Okayama 700-8525, Japan

TEL

0862356721

Email

miyawaki@md.okayama-u.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Shigeru Maeda

Organization

Okayama University Graduate School of Medicine, Dentistry and Parmaceutical Sciences

Division name

Department of Dental Anesthesiology and Special Care Dentistry

Zip code


Address

2-5-1 Shikata-cho, Kita-ku, Okayama, Japan

TEL

0862356721

Homepage URL


Email

miyawaki@md.okayama-u.ac.jp


Sponsor or person

Institute

Okayama University Graduate School of Medicine, Dentistry and Parmaceutical Sciences

Institute

Department

Personal name



Funding Source

Organization

None

Organization

Division

Category of Funding Organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2011 Year 09 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

Completed

Date of protocol fixation

2011 Year 05 Month 24 Day

Date of IRB


Anticipated trial start date

2011 Year 09 Month 01 Day

Last follow-up date

2012 Year 12 Month 31 Day

Date of closure to data entry

2012 Year 12 Month 31 Day

Date trial data considered complete

2012 Year 12 Month 31 Day

Date analysis concluded

2013 Year 01 Month 31 Day


Other

Other related information

Cohort study


Management information

Registered date

2011 Year 08 Month 31 Day

Last modified on

2015 Year 07 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007412


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name