UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000005615
Receipt number R000006634
Scientific Title The study of physiological stress and recovery condition between AOP vs. TIVA for ambulatory general anesthesia to dental patient -Salivary alpha-amylase level and activity of autonomic nervous system were measured for mental retardation and autism patient-
Date of disclosure of the study information 2011/05/17
Last modified on 2014/03/24 09:07:18

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Basic information

Public title

The study of physiological stress and recovery condition between AOP vs. TIVA for ambulatory general anesthesia to dental patient
-Salivary alpha-amylase level and activity of autonomic nervous system were measured for mental retardation and autism patient-

Acronym

The study of physiological stress and recovery condition for ambulatory general anesthesia

Scientific Title

The study of physiological stress and recovery condition between AOP vs. TIVA for ambulatory general anesthesia to dental patient
-Salivary alpha-amylase level and activity of autonomic nervous system were measured for mental retardation and autism patient-

Scientific Title:Acronym

The study of physiological stress and recovery condition for ambulatory general anesthesia

Region

Japan


Condition

Condition

dental patients with mental retardation and/or autism

Classification by specialty

Anesthesiology Dental medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We will be randomized controlled trial for physiological stress and recovery condition between AOP and TIVA for dental procedures. We measure salivary alpha-amylase and heart rate variability for stress, also measure discharge time and PONV for recovery condition.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase IV


Assessment

Primary outcomes

salivary alpha-amylase
discharge time

Key secondary outcomes

heart rate variability
incident of PONV


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Single blind -participants are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

AOP group
Patients receive sevoflurane induction. Then we stop sevoflurane after having venous line and 2mg/kg propofol, 10mg/kg/h rocuronium administer for LMA insertion. They receive 2 l/min air, 1 l/min oxygen and propofol for between BIS 40-60. Zero point one-0.2 mg/kg rocuronium administer when patients move during procedure. Two % lidocalne with adrenaline injection administer if operator need.
Data will have from May 2011 to April 2013 and end of analysis at August 2013.

Interventions/Control_2

TIVA group
Patients receive sevoflurane induction. Then we stop sevoflurane after having venous line and 2mg/kg propofol, 0.5micro g/kg/min remifentanil administer for LMA insertion. They receive either 2l/min air, 1l/min oxygen, 0.2micro g/kg/min remifentanil and propofol for between BIS 40-60. Zero point one-0.2 mg/kg rocuronium administer when patients move during procedure. Two % lidocalne with adrenaline injection administer if operator need.
Data will have from May 2011 to April 2013 and end of analysis at August 2013.

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

ASA class 1 or 2 mental retardation and autism patients who scheduled for dental procedure under general anesthesia.

Key exclusion criteria

Body weight under 10kg
Heart disease over NYHA class 2
Taking psychotropics
Having drug allergy
Cannot take IC of guardian

Target sample size

50


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name sunada katsuhisa

Organization

The nippon dental university

Division name

department of dental anesthesiology

Zip code


Address

1-9-20 fujimi chiyodaku tokyo Japan

TEL

03-3261-8311

Email

katsu.sunada@nifty.com


Public contact

Name of contact person

1st name
Middle name
Last name sunada katsuhisa

Organization

The nippon dental university

Division name

department of dental anesthesiology

Zip code


Address

1-9-20 fujimi chiyodaku tokyo Japan

TEL

03-3261-8311

Homepage URL


Email

katsu.sunada@nifty.com


Sponsor or person

Institute

The nippon dental university

Institute

Department

Personal name



Funding Source

Organization

The nippon dental 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


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

日本歯科大学附属病院(東京都)、東京都障害者口腔保健センター(東京都)、埼玉県歯科医師会口腔保健センター(埼玉県)


Other administrative information

Date of disclosure of the study information

2011 Year 05 Month 17 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 17 Day

Date of IRB


Anticipated trial start date

2011 Year 05 Month 01 Day

Last follow-up date

2013 Year 04 Month 01 Day

Date of closure to data entry

2013 Year 04 Month 01 Day

Date trial data considered complete

2013 Year 04 Month 01 Day

Date analysis concluded

2013 Year 08 Month 01 Day


Other

Other related information



Management information

Registered date

2011 Year 05 Month 17 Day

Last modified on

2014 Year 03 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006634


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name