UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000010026
Receipt number R000011739
Scientific Title Abdominal CT Studies for Newly-Developed Scan and Contrast EnhancementTechniques and Image Analysis Methods
Date of disclosure of the study information 2013/05/01
Last modified on 2013/02/13 17:44:41

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Basic information

Public title

Abdominal CT Studies for Newly-Developed Scan and Contrast EnhancementTechniques and Image Analysis Methods

Acronym

Abdominal CT Studies for Newly-Developed Scan and Contrast EnhancementTechniques and Image Analysis Methods

Scientific Title

Abdominal CT Studies for Newly-Developed Scan and Contrast EnhancementTechniques and Image Analysis Methods

Scientific Title:Acronym

Abdominal CT Studies for Newly-Developed Scan and Contrast EnhancementTechniques and Image Analysis Methods

Region

Japan


Condition

Condition

Abdominal diseases

Classification by specialty

Radiology Adult

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To assess various newly-developed abdominal CT divices and techniques such as area-detector, dual X-ray tube, high-speed shuttle scan, gastro- and colonography, and perfusion scan.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Readers' subjective assessmentof CT images including image contrast, tumor detection ability, and vessel visualization
Objective CT image noise, image contrast, tumor detection ability
Comparison with organ perfusion parameters or iodine concentration and other clinical findings
Comparison with findings on CT gasrto/olonography and other clinical findings

Key secondary outcomes



Base

Study type


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit


Blinding

Double blind -all involved are blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

9

Purpose of intervention

Diagnosis

Type of intervention

Medicine Device,equipment Maneuver

Interventions/Control_1

Area-detector scan

Interventions/Control_2

Dual X-ray tube scan

Interventions/Control_3

High-speed helical shuttle

Interventions/Control_4

respiratory triggered scan

Interventions/Control_5

CT gasrtography and colonography

Interventions/Control_6

Determination of substance in the body

Interventions/Control_7

Organ perfusion measurement

Interventions/Control_8

Dose reduction of contrastmedium

Interventions/Control_9

Dose reduction of irradiation

Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Adult (20 years old or elder) patients who have or are suspeced to have abdominal diseases underwent or will undergo abdominal CT examination in our institution

Key exclusion criteria

None

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Takeshi Yoshikawa

Organization

Kobe University Graduate School of Medicine

Division name

Advanced Biomedical Imaging Research Center/Department of Radiology

Zip code


Address

7-5-2 Kusunokicho Chuoku, Kobe, Hyogo 650-0017 Japan

TEL


Email



Public contact

Name of contact person

1st name
Middle name
Last name

Organization

Kobe University Graduate School of Medicine

Division name

Advanced Biomedical Imaging Research Center/Department of Radiology

Zip code


Address


TEL


Homepage URL


Email



Sponsor or person

Institute

Kobe University Graduate School of Medicine

Institute

Department

Personal name



Funding Source

Organization

Kobe University Graduate School of Medicine

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



Other administrative information

Date of disclosure of the study information

2013 Year 05 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

Preinitiation

Date of protocol fixation

2013 Year 05 Month 01 Day

Date of IRB


Anticipated trial start date

2013 Year 05 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 02 Month 13 Day

Last modified on

2013 Year 02 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000011739


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name