UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019773
Receipt number R000022835
Scientific Title The effect of general anesthesia on the cerebral perfusion time in patients with carotid artery stenosis : A retrospective study
Date of disclosure of the study information 2015/11/13
Last modified on 2020/03/18 15:21:50

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Basic information

Public title

The effect of general anesthesia on the cerebral perfusion time in patients with carotid artery stenosis : A retrospective study

Acronym

The effect of general anesthesia on the cerebral perfusion time in patients with carotid artery stenosis.

Scientific Title

The effect of general anesthesia on the cerebral perfusion time in patients with carotid artery stenosis : A retrospective study

Scientific Title:Acronym

The effect of general anesthesia on the cerebral perfusion time in patients with carotid artery stenosis.

Region

Japan


Condition

Condition

Carotid artery stenosis or occlusion

Classification by specialty

Anesthesiology Neurosurgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To compare the cerebral perfusion time under awake and general anesthesia in patients with carotid artery stenosis .

Basic objectives2

Pharmacodynamics

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Time of the arrival of the contrast medium in the major cerebral vessels (ACA, MCA, OA, Veins) under awake vs propofol or awake vs sevoflurane.

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

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients undergone AG for diagnosis and CAS under general anesthesia in Tokyo Medical and Dental University from Jan. 1, 2012 to Feb 28, 2017.

Key exclusion criteria

Patients who refused the participation of this study

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Shigeru
Middle name
Last name Nemoto

Organization

Tokyo Medical and Dental University,
Graduate School of Medicine and Dental Sciences

Division name

Department of Endovascular Surgery

Zip code

113-8510

Address

1-5-45 Yushima, Bunkyo-ku, Tokyo, JAPAN

TEL

03-5803-5325

Email

nemoto.evs@tmd.ac.jp


Public contact

Name of contact person

1st name Tomoko
Middle name
Last name Ishibashi

Organization

Tokyo Medical and Dental University, Graduate School of Medicine and Dental Sciences

Division name

Department of Anesthesiology

Zip code

113-8510

Address

1-5-45, Yushima, Bunkyo-ku, Tokyo, JAPAN

TEL

03-5803-5325

Homepage URL


Email

timane@tmd.ac.jp


Sponsor or person

Institute

Tokyo Medical and Dental University

Institute

Department

Personal name



Funding Source

Organization

Japan Research Foundation for Clinical Pharmacology

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Tokyo Medical and Dental University

Address

Yushima 1-5-45, Bunkyo-ku, Tokyo, Japan

Tel

03-3813-6111

Email

mkan-rinsho.adm@tmd.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

2015 Year 11 Month 13 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

2015 Year 09 Month 08 Day

Date of IRB

2015 Year 11 Month 02 Day

Anticipated trial start date

2015 Year 11 Month 13 Day

Last follow-up date

2019 Year 04 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Retrospective study
We measure the time of the arrival of the contrast medium from the base line in ICA to each cerebral blood vessels with angiographic image under awake and general anesthesia.


Management information

Registered date

2015 Year 11 Month 13 Day

Last modified on

2020 Year 03 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022835


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name