UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000020300 |
|---|---|
| Receipt number | R000023445 |
| Scientific Title | 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 10:00:17 |
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Basic information
Public title
Effect of Carnitine Treatment on HCV in liver cirrhosis patients with hepatitis C virus infection
Acronym
Effect of Carnitine on HCV
Scientific Title
Effect of Carnitine Treatment on HCV in liver cirrhosis patients with hepatitis C virus infection
Scientific Title:Acronym
Effect of Carnitine on HCV
Region
| Japan |
Condition
Condition
Liver cirrhosis Patients with HCV infection
Classification by specialty
| Hepato-biliary-pancreatic medicine |
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
| 20 | years-old | <= |
Age-upper limit
| Not applicable |
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
| 1st name | |
| Middle name | |
| Last name | Goki Suda |
Organization
Hokkaido University
Division name
Department of Gastroenterology and Hepatology, Graduate School of Medicine,
Zip code
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
| 1st name | |
| Middle name | |
| Last name | Goki Suda |
Organization
Hokkaido University
Division name
Department of Gastroenterology and Hepatology, Graduate School of Medicine,
Zip code
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 or person
Institute
Hokkaido University
Institute
Department
Personal name
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)
IRB Contact (For public release)
Organization
Address
Tel
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
| 2015 | Year | 12 | Month | 21 | Day |
Related information
URL releasing protocol
Publication of results
Unpublished
Result
URL related to results and publications
Number of participants that the trial has enrolled
Results
Results date posted
Results Delayed
Results Delay Reason
Date of the first journal publication of results
Baseline Characteristics
Participant flow
Adverse events
Outcome measures
Plan to share IPD
IPD sharing Plan description
Progress
Recruitment status
Completed
Date of protocol fixation
| 2014 | Year | 05 | Month | 01 | Day |
Date of IRB
Anticipated trial start date
| 2014 | Year | 05 | Month | 01 | Day |
Last follow-up date
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
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
| 2015 | Year | 12 | Month | 21 | Day |
Last modified on
| 2019 | Year | 02 | Month | 14 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023445
