Unique ID issued by UMIN | UMIN000030680 |
---|---|
Receipt number | R000035028 |
Scientific Title | Comprehensive analysis of iron and mineral-bone metabolism after HCV clearance by glecaprevir and pibrentasvir therapy in HCV-infected hemodialysis patients |
Date of disclosure of the study information | 2018/01/04 |
Last modified on | 2022/08/25 13:47:08 |
Comprehensive analysis of iron and mineral-bone metabolism after HCV clearance by glecaprevir and pibrentasvir therapy in HCV-infected hemodialysis patients
Comprehensive analysis of iron and mineral-bone metabolism after HCV clearance by glecaprevir and pibrentasvir therapy in HCV-infected hemodialysis patients
Comprehensive analysis of iron and mineral-bone metabolism after HCV clearance by glecaprevir and pibrentasvir therapy in HCV-infected hemodialysis patients
Comprehensive analysis of iron and mineral-bone metabolism after HCV clearance by glecaprevir and pibrentasvir therapy in HCV-infected hemodialysis patients
Japan |
HCV patients receiving hemodialysis
Hepato-biliary-pancreatic medicine |
Others
NO
we aim at examining the effect on iron and mineral-bone metabolism after HCV clearance by glecaprevir and pibrentasvir therapy in HCV-infected hemodialysis patients
Safety,Efficacy
To compare erythropoietic resistance index change between pre and post of treatment
To assess Iron metabolism kinetics (hepcidin,ferritin,Fe,TIBC)
To assess mineral-bone metabolism kinetics (FGF23,1.25D,25D,intactPTH)
To assess antiviral activity, the proportion of subjects who achieve undetectable HCV RNA at post treatment week 12
To assess safety
To assess CLDQ-HCV, KDQOL-SF
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
Patients will orally receive glecaprevir 300mg and pibrentasvir 120mg once daily for 8 or 12 weeks.
20 | years-old | <= |
Not applicable |
Male and Female
1)20 years old or older
2)HCV-infected(genotype1,2,3,4,5,6) patients with hemodialysis
3)Patients who were provided with sufficient explanation before participating in this study and who provided written consent to participate in this study on their own free will.
1)Patients with decompensated cirrhosis
2)Patients complicated with hepatocellular carcinoma
3)Patients with HBs antigen or anti-HIV antibody positive
4)Patients with a history of hypersensitivity to lecaprevir and pibrentasvir
5)Patients receiving atazanavir sulfate (Reyataz), atorvastatin calcium hydrate (Lipitor etc.), rifampicin (Rifazine etc.)
6)Other patients whom the chief investigator or a sub-investigators considers inappropriate
30
1st name | |
Middle name | |
Last name | Yoshitaka Arase |
Tokai University School of Medicine
Department of Gastroenterology and Hepatology
shimokasuya 143, Isehara, Kanagawa, Japan
0463-93-1121
arase@tokai-u.jp
1st name | |
Middle name | |
Last name | Yoshitaka Arase |
Tokai University Oiso Hospital
Department of Gastroenterology and Hepatology
Gakkyo 21-1, Oisotyo, Nakagun, Kanagawa, Japan
0463-72-3211
arase@tokai-u.jp
Tokai University School of Medicine, Department of Gastroenterology and Hepatology
Tokai University School of Medicine, Department of Gastroenterology and Hepatology
Self funding
NO
東海大学医学部付属病院
東海大学医学部付属大磯病院
東海大学医学部付属八王子病院
東海大学医学部付属東京病院
帝京大学医学部付属病院
順天堂大学医学部付属順天堂医院
順天堂大学医学部付属練馬病院
医療法人社団豊済会 下落合クリニック
医療法人社団松和会 池上総合病院
2018 | Year | 01 | Month | 04 | Day |
Unpublished
Completed
2017 | Year | 12 | Month | 19 | Day |
2017 | Year | 12 | Month | 19 | Day |
2018 | Year | 01 | Month | 04 | Day |
2020 | Year | 12 | Month | 31 | Day |
2018 | Year | 01 | Month | 04 | Day |
2022 | Year | 08 | Month | 25 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035028