UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008851
Receipt number R000010392
Scientific Title Effect of desflurane and propofol on cardiac electrophysiology
Date of disclosure of the study information 2012/09/06
Last modified on 2017/09/09 19:20:11

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Basic information

Public title

Effect of desflurane and propofol on cardiac electrophysiology

Acronym

Effect of desflurane and propofol on cardiac electrophysiology

Scientific Title

Effect of desflurane and propofol on cardiac electrophysiology

Scientific Title:Acronym

Effect of desflurane and propofol on cardiac electrophysiology

Region

Japan


Condition

Condition

Tachyarrhythmia

Classification by specialty

Cardiology Pediatrics Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare the effect of desflurane and propofol on cardiac electrophysiology in children undergoing radiofrequency catheter ablation for tachyarrthythmia

Basic objectives2

Pharmacodynamics

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

sinus node recovery time

Key secondary outcomes

sinoatrial conduction time, atrial-His conduction time, His bundle refractory time, accessory pathway effective refractory time


Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

Active

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

3

Purpose of intervention

Prevention

Type of intervention

Medicine

Interventions/Control_1

general anesthesia with propofol

Interventions/Control_2

general anesthesia with desflurane at low concentration

Interventions/Control_3

general anesthesia with desflurane at high concentration

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

1 years-old <=

Age-upper limit

15 years-old >=

Gender

Male and Female

Key inclusion criteria

Children undergoing radiofrequency catheter ablation for tachyarrhythmia

Key exclusion criteria

Children with other congenital heart disease than tachyarrhythmia and children undergoing surgery other than radiofrequency catheter ablation

Target sample size

60


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Ryu Okutani

Organization

Osaka City General Hospital

Division name

Department of Anesthesiology

Zip code


Address

2-13-22 Miyakojima Hondori, Miyakojima-ku, Osaka

TEL

06-6929-1221

Email

ryuokutani0909@ybb.ne.jp


Public contact

Name of contact person

1st name
Middle name
Last name Ryu Okutani

Organization

Osaka City General Hospital

Division name

Department of Anesthesiology

Zip code


Address

2-13-22 Miyakojima Hondori, Miyakojima-ku, Osaka

TEL

06-6929-1221

Homepage URL


Email

ryuokutani0909@ybb.ne.jp


Sponsor or person

Institute

Department of Anesthesiology, Osaka City General Hospital

Institute

Department

Personal name



Funding Source

Organization

Department of Anesthesiology, Osaka City General Hospital

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

大阪市立総合医療センター麻酔科


Other administrative information

Date of disclosure of the study information

2012 Year 09 Month 06 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

No longer recruiting

Date of protocol fixation

2012 Year 07 Month 01 Day

Date of IRB


Anticipated trial start date

2012 Year 07 Month 10 Day

Last follow-up date

2016 Year 05 Month 31 Day

Date of closure to data entry

2016 Year 06 Month 30 Day

Date trial data considered complete

2016 Year 07 Month 31 Day

Date analysis concluded

2016 Year 09 Month 30 Day


Other

Other related information



Management information

Registered date

2012 Year 09 Month 04 Day

Last modified on

2017 Year 09 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010392


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name