UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019399
Receipt number R000022439
Scientific Title Prospective study of Sofosbuvir/Ribavirin for HCV genotype 2 infected Japanese patients
Date of disclosure of the study information 2015/11/01
Last modified on 2022/05/03 13:28:21

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Basic information

Public title

Prospective study of Sofosbuvir/Ribavirin for HCV genotype 2 infected Japanese patients

Acronym

IFN free SR study

Scientific Title

Prospective study of Sofosbuvir/Ribavirin for HCV genotype 2 infected Japanese patients

Scientific Title:Acronym

IFN free SR study

Region

Japan


Condition

Condition

Genotype 2 infected chronic liver diseases

Classification by specialty

Medicine in general Hepato-biliary-pancreatic medicine

Classification by malignancy

Others

Genomic information

YES


Objectives

Narrative objectives1

Efficacy and safety

Basic objectives2

Others

Basic objectives -Others

viral genome

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

sustained viral response

Key secondary outcomes

Suppression of hepatocarcinogenesis


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

HCV genotype 2 infected patients with chronic liver disorders.
Patients satisfied the public indication for sofosbuvir and ribavirin

Key exclusion criteria

Pregnant women
Decompensated cirrhosis
Hepatocellular carcinoma
Renal impairment (eGFR<30)
Doctors judge as inappropriate

Target sample size

250


Research contact person

Name of lead principal investigator

1st name Akihiro
Middle name
Last name Tamori

Organization

Osaka City University Graduate School of Medicine

Division name

Department of Hepatology

Zip code

5458585

Address

1-4-3, Asahimachi, Abeno-ku, Osaka 545-8585, JAPAN

TEL

06-6645-3811

Email

atamori@med.osaka-cu.ac.jp


Public contact

Name of contact person

1st name Akihiro
Middle name
Last name Tamori

Organization

Osaka City University Graduate School of Medicine

Division name

Department of Hepatology

Zip code

5458585

Address

1-4-3, Asahimachi, Abeno-ku, Osaka 545-8585, JAPAN

TEL

06-6645-3811

Homepage URL


Email

atamori@med.osaka-cu.ac.jp


Sponsor or person

Institute

Osaka City University and affiliated hospitals

Institute

Department

Personal name



Funding Source

Organization

Osaka City 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

The ethical committee, Osaka City University Hospital

Address

1-4-3, Asahimachi, Abeno-ku, Osaka 545-8585, JAPAN

Tel

06-6645-3435

Email

ethics@med.osaka-cu.ac.jp


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



Other administrative information

Date of disclosure of the study information

2015 Year 11 Month 01 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

2015 Year 07 Month 28 Day

Date of IRB

2015 Year 06 Month 02 Day

Anticipated trial start date

2015 Year 08 Month 01 Day

Last follow-up date

2021 Year 12 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Patients treated with SOF/RBV from June 1 2015 to December 31 2018
Examination for HCV viral load, AFP, and M2BPGi


Management information

Registered date

2015 Year 10 Month 19 Day

Last modified on

2022 Year 05 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022439


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name