Unique ID issued by UMIN | UMIN000005598 |
---|---|
Receipt number | R000004266 |
Scientific Title | Trial of novel combined therapy between interferon and hyperlipidemia for chronic hepatitis C patients |
Date of disclosure of the study information | 2011/05/13 |
Last modified on | 2011/05/13 15:59:25 |
Trial of novel combined therapy between interferon and hyperlipidemia for chronic hepatitis C patients
Novel combined therapy for chronic hepatitis C patients
Trial of novel combined therapy between interferon and hyperlipidemia for chronic hepatitis C patients
Novel combined therapy for chronic hepatitis C patients
Japan |
chronic hepatitis type C
Hepato-biliary-pancreatic medicine | Endocrinology and Metabolism |
Others
NO
We estimate safety as the effectiveness of the peginterferon alpha-2a (following PEG-IFN), Ribavirin (following RBV) and fluvastatin combination therapy for the chronic hepatitis C patient having the fatty liver.
Safety,Efficacy
Confirmatory
Phase III
SVR rate(HCV RNA lasting negative)
SBR rate(ALT lasting normalization),the timing HCV RNA negative and adverse event
Interventional
Parallel
Randomized
Individual
Single blind -participants are blinded
Active
YES
YES
Institution is not considered as adjustment factor.
NO
Central registration
2
Treatment
Medicine |
Group A Fluvastatin(LOCHOL Tablets) 20~30mg/day is administered 12 weeks alone(The example of seriousness administers 60mg in the maximum).
Afterwards, administering of using together is done by the amount corresponding to weight it as for PEG-IFN (Pegasys)(once a week)and RBV(Copegas)(every day).
The HCV-RNA density in blood is measured once a month. Administering is extended until 72 weeks if it will not make gloomily by 12 weeks, and it will make it gloomily by 36 weeks.
Afterwards, it takes withdraw for 24 weeks, and the effect is judged.
Group B Administering of using together is done by the amount corresponding to weight it as for PEG-IFN (Pegasys)(once a week)and RBV(Copegas)(every day).
The HCV-RNA density in blood is measured once a month. Administering is extended until 72 weeks if it will not make gloomily by 12 weeks, and it will make it gloomily by 36 weeks.
Afterwards, it takes withdraw for 24 weeks, and the effect is judged.
Not applicable |
Not applicable |
Male and Female
Patient who applies to eligibility criteria for* by chronic hepatitis C (
Serogroup1(genotype1b)and the viral load in blood is HCV-RNA 5.0LogIU/ml or more).
*Patient with chronicity C type chronic hepatitis to which treatment resistance is expected by disorder of lipid metabolism(Patient who meets requirement more than one item either the following)
1.Triglyceride value 150mg/dL or more
2.Less than HDL cholesterol value 40mg/dL
3.Area 100cm3 or more of visceral fat
4.The female 25%or more by the body fat percentage man 22% or more.
100
1st name | |
Middle name | |
Last name | yoshiki murakami |
Kyoto University Graduate School of Medicine
Center for Genomic Medicine
kyotoshi sakyouku shougoin kawaharatyou53
075-751-4192
1st name | |
Middle name | |
Last name | yoshiki murakami |
Kyoto University Graduate School of Medicine
Center for Genomic Medicine
kyotoshi sakyouku shougoin kawaharatyou53
075-751-4192
ymurakami@genome.kyoto-u.ac.jp
Kyoto University Graduate School of Medicine
Center for Genomic Medicine
kagakukenkyuuhi
Japan
NO
2011 | Year | 05 | Month | 13 | Day |
Unpublished
Open public recruiting
2010 | Year | 07 | Month | 16 | Day |
2010 | Year | 09 | Month | 01 | Day |
2014 | Year | 07 | Month | 01 | Day |
2011 | Year | 05 | Month | 13 | Day |
2011 | Year | 05 | Month | 13 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000004266