Unique ID issued by UMIN | UMIN000040727 |
---|---|
Receipt number | R000046494 |
Scientific Title | The crossover randomized controlled clinical trial with Alirocumab and Evolocumab:CROSS ALIVE Study |
Date of disclosure of the study information | 2020/06/12 |
Last modified on | 2025/05/12 17:25:06 |
The crossover randomized controlled clinical trial with Alirocumab and Evolocumab:CROSS ALIVE Study
The crossover randomized controlled clinical trial with Alirocumab and Evolocumab:CROSS ALIVE Study
The crossover randomized controlled clinical trial with Alirocumab and Evolocumab:CROSS ALIVE Study
The crossover randomized controlled clinical trial with Alirocumab and Evolocumab:CROSS ALIVE Study
Japan |
The crossover randomized controlled clinical trial with Alirocumab and Evolocumab:CROSS ALIVE Study
Medicine in general |
Others
NO
The crossover randomized controlled clinical trial with Alirocumab and Evolocumab
Others
Changes in LDL quantity and quality depending on the degree of LDL decline
Exploratory
Explanatory
Phase IV
Lipid profile (TC,TG,HDL-C, Friedewald LDL-C,small dense LDL,IDL,Lp(a),LDL oxidation ability,LDL stability,oxidized LDL,3%PAGE,Agarose gel electrophoresis,electronegative LDL),apo protein, apoE phenotype, Ultracentrifugation, gel filtration, ion exchange chromatography
Cr, BUN, Urinal analysis, GOT, GPT, CK, (following in the case of DM), fasting blood glucose, HbA1, hematologic changes such as thrombocytopenia, etc., early-phase and late-phase of allergic reaction to PCSK9 inhibitor.
Interventional
Cross-over
Randomized
Individual
Open -no one is blinded
Active
YES
YES
Institution is not considered as adjustment factor.
YES
Pseudo-randomization
2
Treatment
Medicine |
Before switching from 75 mg, 150 mg arilocumab to 140 mg, 420 mg evolocumab, and 3 months after the switch.
Before switching from 140 mg, 420 mg evolocumab to 75 mg, 150 mg arilocumab, and 3 months after the switch.
20 | years-old | <= |
Not applicable |
Male and Female
1)-3) 3 examine group
1)T2DM with 120 mg/dl or more than 100 mg/dl LDL-C
2)Patients of JAS Guidelines for Prevention of Atherosclerotic Cardiovascular Diseases 2017 CategoryIII (Diabetes patients are excepted) with 120 mg/dl or more than 100 mg/dl LDL-C
3)Patients of JAS Guidelines for Prevention of Atherosclerotic Cardiovascular Diseases 2017 Secondary prevention with 100 mg/dl or more than 70 mg/dl LDL-C
A patient with the side-effects past in statin medication
20
1st name | Ikuo |
Middle name | |
Last name | Inoue |
Saitama Medical University
Dept. of Endocrinology and Diabetology
350-0495
38 Morohongo, Moroyama-machi, Iruma-gun, Saitama
049-276-1875
i1901018@saitama-med.ac.jp
1st name | Ikuo |
Middle name | |
Last name | Inoue |
Saitama Medical University
Dept. of Endocrinology and Diabetology
350-0495
38 Morohongo, Moroyama-machi, Iruma-gun, Saitama
049-276-1875
i1901018@saitama-med.ac.jp
Saitama Medical University
Dept. of Endocrinology and Diabetology
Saitama Medical University
Dept. of Endocrinology and Diabetology
Other
Saitama Medical University Dept. of Endocrinology and Diabetology
38 Morohongo, Moroyama-machi, Iruma-gun, Saitama
049-276-1204
i1901018@saitama-med.ac.jp
NO
2020 | Year | 06 | Month | 12 | Day |
Unpublished
Open public recruiting
2020 | Year | 06 | Month | 11 | Day |
2020 | Year | 07 | Month | 01 | Day |
2025 | Year | 01 | Month | 01 | Day |
2030 | Year | 12 | Month | 31 | Day |
2035 | Year | 12 | Month | 31 | Day |
2035 | Year | 12 | Month | 31 | Day |
2035 | Year | 12 | Month | 31 | Day |
2020 | Year | 06 | Month | 11 | Day |
2025 | Year | 05 | Month | 12 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046494