UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000051688
Receipt number R000058595
Scientific Title Preliminary study evaluating renal fibrosis with 18F-FAPI-74 PET imaging, pathology, and clinical findings
Date of disclosure of the study information 2023/07/24
Last modified on 2023/08/17 08:27:50

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Basic information

Public title

Preliminary study evaluating renal fibrosis with 18F-FAPI-74 PET imaging, pathology, and clinical findings

Acronym

FAPIKIDN1

Scientific Title

Preliminary study evaluating renal fibrosis with 18F-FAPI-74 PET imaging, pathology, and clinical findings

Scientific Title:Acronym

FAPIKIDN1

Region

Japan


Condition

Condition

Kidney disease

Classification by specialty

Nephrology Radiology Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To elucidate the pathogenesis of renal fibrosis by examining the relationship between renal 18F-FAPI-74 uptake, pathological indices of renal fibrosis, and related indices of renal function.

Basic objectives2

Others

Basic objectives -Others

Evaluating pathogenesis

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Relationship between renal 18F-FAPI-74 uptake and pathologic renal fibrosis indices

Key secondary outcomes

1. Relationship between renal 18F-FAPI-74 uptake and FAP immunohistochemical findings
2. Relationship between renal 18F-FAPI-74 uptake and renal function (eGFRcys)


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Self control

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Prevention

Type of intervention

Medicine Device,equipment

Interventions/Control_1

18F-FAPI-74 PET/CT

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. Those who are 18 years of age or older at the time of consent
2. Those who have undergone or will undergo a renal biopsy for the purpose of investigation of the renal disease as part of routine medical care within 30 days of the 18F-FAPI-74 PET/CT
3. Those who have undergone or will undergo an eGFRcys (cystatin C) blood test to evaluate renal disease for the purpose of investigation of the renal disease as part of routine medical care within 30 days of the 18F-FAPI-74 PET/CT
4. Those who can obtain written informed consent

Key exclusion criteria

1. Those who are or may be pregnant
2. Those who have undergone or will undergo treatment for the disease between the 18F-FAPI-74 PET/CT and renal biopsy
3. Patients for whom furosemide administration is considered inappropriate by the referring physician
4. Patients for whom water intake is considered inappropriate by the referring physician
5. Those who are with severe claustrophobia
6. Those who are considered to be inappropriate to participate in this study by the principal investigator or sub-investigator

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Tomohiko
Middle name
Last name Yamane

Organization

Kobe City Medical Center General Hospital

Division name

Molecular Imaging Research

Zip code

650-0047

Address

Minatojima-Minamimachi 2-1-1, Chuo-ku, Kobe

TEL

078-302-4321

Email

tomohiko_yamane@kcho.jp


Public contact

Name of contact person

1st name Tomohiko
Middle name
Last name Yamane

Organization

Kobe City Medical Center General Hospital

Division name

Molecular Imaging Research

Zip code

650-0047

Address

Minatojima-Minamimachi 2-1-1, Chuo-ku, Kobe

TEL

078-302-4321

Homepage URL

https://chuo.kcho.jp/department/molecular_imaging_research/

Email

tomohiko_yamane@kcho.jp


Sponsor or person

Institute

Kobe City Medical Center General Hospital

Institute

Department

Personal name



Funding Source

Organization

Katakami Foundation For Clinical Research, KBIC Research Grants-in-Aid for Clinical Research Promotion, Self-funding

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kobe City Medical Center General Hospital Research Ethics Committee

Address

Minatojima-Minamimachi 2-1-1, Chuo-ku, Kobe

Tel

078-302-5176

Email

rinken@kcho.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

2023 Year 07 Month 24 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

Enrolling by invitation

Date of protocol fixation

2023 Year 07 Month 03 Day

Date of IRB

2023 Year 08 Month 10 Day

Anticipated trial start date

2023 Year 08 Month 10 Day

Last follow-up date

2025 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2023 Year 07 Month 22 Day

Last modified on

2023 Year 08 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000058595


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name