| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000016069 |
| Receipt No. | R000017200 |
| Official scientific title of the study | Reduction of radiation exposure and contrast material volume in coronary CT angiography with low tube voltage and iterative reconstruction technique |
| Date of disclosure of the study information | 2015/01/01 |
| Last modified on | 2017/08/04 (Ver. 4) |
| Basic information | ||
| Official scientific title of the study | Reduction of radiation exposure and contrast material volume in coronary CT angiography with low tube voltage and iterative reconstruction technique | |
| Title of the study (Brief title) | Reduction of radiation exposure and contrast material volume in coronary CT angiography with low tube voltage and iterative reconstruction technique | |
| Region |
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| Condition | |||
| Condition | Coronary artery disease | ||
| Classification by specialty |
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| Classification by malignancy | Others | ||
| Genomic information | NO | ||
| Objectives | |
| Narrative objectives1 | To compare the image quality between conventional coronary CT angiography (CCTA) and CCTA with reduced radiation dose and reduced contrast material volume using low tube voltage and iterative reconstruction technique. |
| Basic objectives2 | Others |
| Basic objectives -Others | Reduction of radiation exposure and contrast material volume in coronary CT angiography |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | image quality |
| Key secondary outcomes | |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Cross-over |
| Randomization | Randomized |
| Randomization unit | |
| Blinding | Open -but assessor(s) are blinded |
| Control | Active |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | ||
| No. of arms | 2 | |
| Purpose of intervention | Diagnosis | |
| Type of intervention |
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| Interventions/Control_1 | Conventional coronary CT angiography | |
| Interventions/Control_2 | Coronary CT angiography with reduced radiation exposure and reduced contrast material volume using low tube voltage and iterative reconstruction technique | |
| 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 |
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| Age-upper limit |
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| Gender | Male and Female | |||
| Key inclusion criteria | 1. Age equal to or more than 20 years
2. Scheduled to undergo a clinically indicated coronary CT angiography 3. Heart rate at coronary CT andiography equal to or lower than 65/min |
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| Key exclusion criteria | 1. Prior coronary artery bypass graft (CABG) surgery
2. Contraindication to beta blocker agents or nitrates 3. Recent prior myocardial infarction 4. Prior pacemaker or internal defibrillator lead implantation 5. Tachycardia or significant arrhythmia 6. Impaired chronic renal function (serum creatinine >1.5 mg/dl) 7. Subjects with known anaphylactic allergy to iodinated contrast material 8. Pregnancy or unknown pregnancy status in subject of childbearing potential 9. Subject requires an emergent procedure |
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| Target sample size | 50 | |||
| Research contact person | |
| Name of lead principal investigator | Masahiro Jinzaki |
| Organization | Keio University School of Medicine |
| Division name | Department of Diagnostic Radiology |
| Address | 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan |
| TEL | 03-3353-1211(+81-3-3353-1211) |
| jinzaki@rad.med.keio.ac.jp | |
| Public contact | |
| Name of contact person | Yoshitake Yamada |
| Organization | Keio University School of Medicine |
| Division name | Department of Diagnostic Radiology |
| Address | 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan |
| TEL | 03-3353-1211(+81-3-3353-1211) |
| Homepage URL | |
| yamada@rad.med.keio.ac.jp | |
| Sponsor | |
| Institute | Keio University |
| Institute | |
| Department | |
| Funding Source | |
| Organization | GE Healthcare |
| Organization | |
| Division | |
| Category of Funding Organization | Profit organization |
| Nationality of Funding Organization | |
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| Co-sponsor | |
| Name of secondary funder(s) | |
| 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 | |
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| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | Completed | ||||||
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| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| URL releasing results | |
| Results | |
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| Management information | |||||||
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000017200 |