| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000020300 |
| Receipt No. | R000023445 |
| Official scientific title of the study | Effect of Carnitine Treatment on HCV in liver cirrhosis patients with hepatitis C virus infection |
| Date of disclosure of the study information | 2015/12/21 |
| Last modified on | 2019/02/14 (Ver. 3) |
| Basic information | ||
| Official scientific title of the study | Effect of Carnitine Treatment on HCV in liver cirrhosis patients with hepatitis C virus infection | |
| Title of the study (Brief title) | Effect of Carnitine on HCV | |
| Region |
|
|
| Condition | ||
| Condition | Liver cirrhosis Patients with HCV infection | |
| Classification by specialty |
|
|
| Classification by malignancy | Others | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | To evaluate the virological and biochemical effect of carnitine administration in patients with a chronic HCV infection |
| Basic objectives2 | Safety,Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | Change of serum HCV titer |
| Key secondary outcomes | ) Change of oxidant stress maker and blood biochemistry
2) Presence or absence of a reversal of liver fibrosis 3) Presence or absence of an improvement in AFP levels 4) Effects of glucose/lipid-related factors on treatment response 5) Incidence of AEs |
| 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 |
|
|||
| Age-upper limit |
|
|||
| Gender | Male and Female | |||
| Key inclusion criteria |
[1] Patients who are 20 years of age or older at the time of informed consent [2] Patients who have been fully informed and have provided written informed consent to participate in this study prior to study initiation [3] Patients with a chronic HCV infection who do not meet any of the following exclusion criteria |
|||
| Key exclusion criteria | 1) Patients with poorly controlled cardiac disease (e.g., myocardial infarction, cardiac failure, arrhythmia)
2) Patients with severe hepatic impairment 3) Patients with a concurrent malignancy, including hepatocellular carcinoma, at the start of treatment 4) Patients who are unsuitable, in the opinion of the principal investigator, for this study due to any other reason |
|||
| Target sample size | 50 | |||
| Research contact person | |
| Name of lead principal investigator | Goki Suda |
| Organization | Hokkaido University |
| Division name | Department of Gastroenterology and Hepatology, Graduate School of Medicine, |
| Address | Kita 14-jo Nishi 5-jo, Kita-ku, Sapporo city, Hokkaid |
| TEL | +81-11-716-1161 |
| gsudgast@pop.med.hokudai.ac.jp | |
| Public contact | |
| Name of contact person | Goki Suda |
| Organization | Hokkaido University |
| Division name | Department of Gastroenterology and Hepatology, Graduate School of Medicine, |
| Address | Kita 14-jo Nishi 5-jo, Kita-ku, Sapporo city, Hokkaid |
| TEL | +81-11-716-1161 |
| Homepage URL | |
| gsudgast@pop.med.hokudai.ac.jp | |
| Sponsor | |
| Institute | Hokkaido University |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Hokkaido University |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | |
| Other related organizations | |
| 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 | |
| Institutions | 北海道大学病院(北海道) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
|
||||||
| Progress | |||||||
| Recruitment status | Completed | ||||||
| Date of protocol fixation |
|
||||||
| Anticipated trial start date |
|
||||||
| Last follow-up date | |||||||
| Date of closure to data entry | |||||||
| Date trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| URL releasing results | |
| Results | |
| Other related information | This study is cohort study
Way for subscription Patients who visit our hospital between May 2014 and march 2018, and meet inclusion criteria are enrolled. |
| Management information | |||||||
| Registered date |
|
||||||
| Last modified on |
|
||||||
| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023445 |