UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040545
Receipt number R000046282
Scientific Title Risk assessment of hepatitis B virus reactivation in renal transplant patient
Date of disclosure of the study information 2020/05/27
Last modified on 2022/03/10 15:01:44

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Basic information

Public title

Risk assessment of hepatitis B virus reactivation in renal transplant patient

Acronym

HBV reactivation in renal transplant patient

Scientific Title

Risk assessment of hepatitis B virus reactivation in renal transplant patient

Scientific Title:Acronym

HBV reactivation in renal transplant patient

Region

Japan


Condition

Condition

hepatitis B virus
renal transplant patient

Classification by specialty

Hepato-biliary-pancreatic medicine Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to assess HBV reactivation in renal transplant patients

Basic objectives2

Others

Basic objectives -Others

To analyze the occurrence rate of HBV reactivation in each status of HBV infection

Trial characteristics_1

Confirmatory

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

To analyze the occurrence rate of HBV reactivation in renal transplant patients

Key secondary outcomes



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 obtaining informed consent
2..Patients who are informed and have provided written informed consent to participate in the study prior to study initiation
3. Renal donor who do not meet any of the following exclusion criteria
4.Renal recipient who do not meet any of the following exclusion criteria

Key exclusion criteria

1.Patients with difficult controlled cardiac disease
2.Patients by whom doctor in charge has determined to be inappropriate as a subject
3.Patients by whom principal investigator has determined to be inappropriate as a subject

Target sample size

500


Research contact person

Name of lead principal investigator

1st name Kiyohiko
Middle name
Last name Hotta

Organization

Hokkaido University Hospital

Division name

Department of Renal and Genitourinary surgery

Zip code

060-8648

Address

KIta 15, NIshi 7, Kita-ku, Sapporo-shi, Hokkaido, Japan

TEL

011-706-5772

Email

hotta1125@mac.com


Public contact

Name of contact person

1st name Kiyohiko
Middle name
Last name Hotta

Organization

Hokkaido University Hospital

Division name

Department of Renal and Genitourinary surgery

Zip code

060-8648

Address

KIta 15, NIshi 7, Kita-ku, Sapporo-shi, Hokkaido, Japan

TEL

011-706-5772

Homepage URL

https://toms.med.hokudai.ac.jp/

Email

hotta1125@mac.com


Sponsor or person

Institute

Department of Renal and Genitourinary surgery
Hokkaido University Hospital

Institute

Department

Personal name



Funding Source

Organization

Department of Renal and Genitourinary surgery
Hokkaido 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

Hokkaido University Hospital Division of Clinical Research Administration

Address

KIta 15, NIshi 7, Kita-ku, Sapporo-shi, Hokkaido, Japan

Tel

011-716-1161

Email

crjimu@huhp.hokudai.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

北海道大学病院(北海道)


Other administrative information

Date of disclosure of the study information

2020 Year 05 Month 27 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

2019 Year 08 Month 20 Day

Date of IRB

2019 Year 09 Month 04 Day

Anticipated trial start date

2019 Year 09 Month 05 Day

Last follow-up date

2035 Year 03 Month 31 Day

Date of closure to data entry

2035 Year 04 Month 01 Day

Date trial data considered complete

2035 Year 05 Month 31 Day

Date analysis concluded

2036 Year 03 Month 31 Day


Other

Other related information

Observation study


Management information

Registered date

2020 Year 05 Month 27 Day

Last modified on

2022 Year 03 Month 10 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000046282


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name