UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000040061
Receipt number R000045636
Scientific Title LIquid biopsy for suspicious LTmphoma patients with Fever Of Unknown oRigin
Date of disclosure of the study information 2020/04/16
Last modified on 2021/04/07 09:03:24

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Basic information

Public title

LIquid biopsy for suspicious LTmphoma patients with Fever Of Unknown oRigin

Acronym

LILY4 Study

Scientific Title

LIquid biopsy for suspicious LTmphoma patients with Fever Of Unknown oRigin

Scientific Title:Acronym

LILY4 Study

Region

Japan


Condition

Condition

Suspicious lymphoma patients with fever of unknown origin

Classification by specialty

Medicine in general Hematology and clinical oncology

Classification by malignancy

Malignancy

Genomic information

YES


Objectives

Narrative objectives1

We assessed the diagnostic efficacy of liquid biopsy for suspicious lymphoma patients with fever of unknown origin.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Concordance rate for diagnosis between liquid biopsy and final diagnosis in FUO.

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) Temperature above 38 over a period of more than 3 weeks.
2) The patients have no effectiveness with antibiotics .
3) Hematologist suspect the lymphoma for FUO without lymphoadenopathy and solid mass.
4) LDH >= a normal level.
5) Twenty years old or higher age.

Key exclusion criteria

1) The patients who were detected the reason of fever.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Akinao
Middle name
Last name Okamoto

Organization

Fujita Health University School of Medicine

Division name

Hematology

Zip code

470-1192

Address

1-98, Dengakugakubo, Kutsukake-cho, Toyoake

TEL

0562-93-9243

Email

aokamoto@fujita-hu.ac.jp


Public contact

Name of contact person

1st name Akinao
Middle name
Last name Okamoto

Organization

Fujita Health University School of Medicine

Division name

Hematology

Zip code

470-1192

Address

1-98, Dengakugakubo, Kutsukake-cho, Toyoake

TEL

0562-93-9243

Homepage URL


Email

aokamoto@fujita-hu.ac.jp


Sponsor or person

Institute

Fujita Health University School of Medicine

Institute

Department

Personal name



Funding Source

Organization

japan Science and Technology Agency

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Fujita Health University School of Medicine

Address

1-98, Dengakugakubo, Kutsukake-cho, Toyoake

Tel

0562-93-2000

Email

kenshien@fujita-hu.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

2020 Year 04 Month 16 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 07 Month 01 Day

Date of IRB

2019 Year 07 Month 19 Day

Anticipated trial start date

2019 Year 09 Month 01 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Observation Study


Management information

Registered date

2020 Year 04 Month 05 Day

Last modified on

2021 Year 04 Month 07 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045636


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name