UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000028440
Receipt number R000032536
Scientific Title Efficacy and safety of medical treatment for advanced hepatocellular carcinoma
Date of disclosure of the study information 2017/07/29
Last modified on 2019/06/22 16:23:36

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Basic information

Public title

Efficacy and safety of medical treatment for advanced hepatocellular carcinoma

Acronym

Medical treatment for HCC

Scientific Title

Efficacy and safety of medical treatment for advanced hepatocellular carcinoma

Scientific Title:Acronym

Medical treatment for HCC

Region

Japan


Condition

Condition

Hepatocellular carcinoma

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the efficacy and safety of medical treatment for advanced hepatocellular carcinoma.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Overall survival

Key secondary outcomes

Time to progression, Progression-free survival, anti-tumor effect, adverse event, complication, prognostic factor, predictive factor


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

Clinically or pathologically diagnosed hepatocellular carcinoma
Twenty or more years old
Written informed consent

Key exclusion criteria

Mental disorder
Inappropriate for paticipating the clinical study

Target sample size

200


Research contact person

Name of lead principal investigator

1st name Tatsuya
Middle name
Last name Yamashita

Organization

Kanazawa University Hospital

Division name

Department of Gastroenterology

Zip code

920-8641

Address

13-1, Takaramachi, Kanazawa

TEL

076-265-2235

Email

ytatsuya@m-kanazawa.jp


Public contact

Name of contact person

1st name Takeshi
Middle name
Last name Terashima

Organization

Kanazawa University Hospital

Division name

Department of Gastroenterology

Zip code

920-8641

Address

13-1, Takaramachi, Kanazawa

TEL

076-265-2235

Homepage URL


Email

tera@m-kanazawa.jp


Sponsor or person

Institute

Kanazawa University Hospital

Institute

Department

Personal name



Funding Source

Organization

Kanazawa University Hospital

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

Certified Review Board, Kanazawa University

Address

13-1, Takaramachi, Kanazawa

Tel

076-265-2834

Email

hpsangak@adm.kanazawa-u.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

2017 Year 07 Month 29 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

Open public recruiting

Date of protocol fixation

2017 Year 06 Month 22 Day

Date of IRB

2017 Year 05 Month 24 Day

Anticipated trial start date

2017 Year 06 Month 22 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Collect information about clinical, radiological, pathological, molecularbiological, and immunological findings of the patients, and investigate the impact of these factors on safety and efficacy of medical treatment for hepatocellular carcinoma.


Management information

Registered date

2017 Year 07 Month 29 Day

Last modified on

2019 Year 06 Month 22 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000032536


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name