UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000006677 |
|---|---|
| Receipt number | R000007889 |
| Scientific Title | Clinical feasibility of newly developed CT reconstruction algorithms |
| Date of disclosure of the study information | 2011/11/07 |
| Last modified on | 2021/05/15 10:11:57 |
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Basic information
Public title
Clinical feasibility of newly developed CT reconstruction algorithms
Acronym
Clinical feasibility of newly developed CT reconstruction algorithms
Scientific Title
Clinical feasibility of newly developed CT reconstruction algorithms
Scientific Title:Acronym
Clinical feasibility of newly developed CT reconstruction algorithms
Region
| Japan |
Condition
Condition
Diseases that images are used for detection, diagnosis, and clinical management
Classification by specialty
| Medicine in general | Gastroenterology | Hepato-biliary-pancreatic medicine |
| Cardiology | Pneumology | Endocrinology and Metabolism |
| Hematology and clinical oncology | Nephrology | Neurology |
| Clinical immunology | Psychosomatic Internal Medicine | Infectious disease |
| Geriatrics | Surgery in general | Gastrointestinal surgery |
| Hepato-biliary-pancreatic surgery | Vascular surgery | Chest surgery |
| Endocrine surgery | Breast surgery | Obstetrics and Gynecology |
| Pediatrics | Ophthalmology | Dermatology |
| Psychiatry | Oto-rhino-laryngology | Orthopedics |
| Urology | Radiology | Anesthesiology |
| Oral surgery | Neurosurgery | Cardiovascular surgery |
| Plastic surgery | Aesthetic surgery | Laboratory medicine |
| Operative medicine | Emergency medicine | Blood transfusion |
| Intensive care medicine | Rehabilitation medicine | Dental medicine |
| Adult | Child |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
To assess clinical feasibility of newly developed CT reconstruction algorithms
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Clinical feasibility of newly developed CT reconstruction algorithms
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
Patients/subjects who are able to give written informed consent
Key exclusion criteria
Patients/subjects who are unable to give written informed consent
Target sample size
500
Research contact person
Name of lead principal investigator
| 1st name | Jiro |
| Middle name | |
| Last name | Sato |
Organization
The University of Tokyo
Division name
Department of Radiology
Zip code
1138655
Address
7-3-1, Hongo, Bunkyo, Tokyo
TEL
03-5800-8666
jsato-tky@umin.ac.jp
Public contact
Name of contact person
| 1st name | Jiro |
| Middle name | |
| Last name | Sato |
Organization
The University of Tokyo
Division name
Department of Radiology
Zip code
1138655
Address
7-3-1, Hongo, Bunkyo, Tokyo
TEL
03-5800-8666
Homepage URL
jsato-tky@umin.ac.jp
Sponsor or person
Institute
Department of Radiology, the University of Tokyo
Institute
Department
Personal name
Funding Source
Organization
Department of Radiology, the University of Tokyo
Organization
Division
Category of Funding Organization
Other
Nationality of Funding Organization
Other related organizations
Co-sponsor
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Department of Radiology, the University of Tokyo
Address
7-3-1, Hongo, Bunkyo, Tokyo
Tel
03-5800-8666
jsato-tky@umin.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
| 2011 | Year | 11 | Month | 07 | Day |
Related information
URL releasing protocol
Publication of results
Partially published
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 | 03 | Month | 01 | Day |
Date of IRB
| 2011 | Year | 03 | Month | 01 | Day |
Anticipated trial start date
| 2011 | Year | 03 | Month | 01 | Day |
Last follow-up date
| 2021 | Year | 03 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
prospective study
Management information
Registered date
| 2011 | Year | 11 | Month | 07 | Day |
Last modified on
| 2021 | Year | 05 | Month | 15 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000007889
