UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018756
Receipt number R000021690
Scientific Title Japan Agency for Medical Research and Development, AMED. Practical Research Project for Rare/Intractable Diseases, Advancing Care of Primary Aldosteronism in Japan Study
Date of disclosure of the study information 2015/08/25
Last modified on 2019/08/26 16:21:28

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Basic information

Public title

Japan Agency for Medical Research and Development, AMED. Practical Research Project for Rare/Intractable Diseases,
Advancing Care of Primary Aldosteronism in Japan Study

Acronym

Japan Primary Aldosteronism Study (JPAS)

Scientific Title

Japan Agency for Medical Research and Development, AMED. Practical Research Project for Rare/Intractable Diseases,
Advancing Care of Primary Aldosteronism in Japan Study

Scientific Title:Acronym

Japan Primary Aldosteronism Study (JPAS)

Region

Japan


Condition

Condition

Primary Aldosteronsim: PA

Classification by specialty

Medicine in general Cardiology Endocrinology and Metabolism
Nephrology Endocrine surgery Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To improve quality of clinical practice of PA and to establish evidence for the clinical guideline of severe form of PA based on 3 clinical questions as followed;
1) prediction score for subtype diagnosis of PA by non-invasive methods,2) standard protocol and decision criteria of adrenal venous sampling(AVS), 3) difference of the effects between surgical and medical treatments of PA, 4)development of highological biomarkers for diagnosis

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Others

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

1) baseline informations(age, sex, duration of hypertension, family history, past history, comorbidity, medications, symptoms, height, weight, blood pressure, pulse rate), biochemical data, results of confirmatory testing, CT
2) protocol and decision criteria of AVS
3) effects of surgical and medical treatment of PA
4) post-operative outcomes

Key secondary outcomes

1)Pathological findings
2)Markers of target organ damage:Kidney(eGFR,BUN,Cr),Heart(ECG,CTR)
3)Clinical course(6M,1Y,3Y,5Y):base line informations, Laboratory data
4)Immunohistochemical staining


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

90 years-old >=

Gender

Male and Female

Key inclusion criteria

Patients who were diagnosed as PA and underwent AVS between January 2006 and Dec 2017 in Kyoto Medical Center and JPAS participating centers

Key exclusion criteria

Patients who were judged not eligible for the study by respective attending physician

Target sample size

3500


Research contact person

Name of lead principal investigator

1st name Naruse
Middle name
Last name Mitsuhide

Organization

National Hospital Organization, Kyoto Medical Center

Division name

Clinical Research Institute for Endocrine and Metabolic Diseases

Zip code

612-8555

Address

1-1Fukakusa-Mukaihatacho, Fushimiku, Kyoto, 612-8555, Japan

TEL

075-641-9161

Email

japan.pa.registry@gmail.com


Public contact

Name of contact person

1st name Naruse
Middle name
Last name Mitsuhide

Organization

National Hospital Organization, Kyoto Medical Center

Division name

Clinical Research Institute for Endocrine and Metabolic Disorders

Zip code

612-8555

Address

1-1Fukakusa-Mukaihatacho, Fushimiku, Kyoto, 612-8555, Japan

TEL

075-641-9161

Homepage URL

http://portal.e-trial.co.jp/adrenal/

Email

japan.pa.registry@gmail.com


Sponsor or person

Institute

National Hospital Organization, Kyoto Medical Center

Institute

Department

Personal name



Funding Source

Organization

Japan Agency for Medical Research and Development, AMED. Practical Research Project for Rare/Intractable Diseases

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

National Hospital Organization, Kyoto Medical Center

Address

1-1Fukakusa-Mukaihatacho, Fushimiku, Kyoto, 612-8555, Japan

Tel

075-641-9161

Email

japan.pa.registry@gmail.com


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

国立病院機構京都医療センター(京都)
聖マリアンナ医科大学(神奈川)       
大阪大学(大阪)         
大分大学(大分)           
應義塾大学(東京)            
京都大学(京都)       
東京医科歯科大学(東京)          
群馬大学(群馬)            
熊本大学(熊本)            
東京大学(東京)            
金沢大学(金沢)        
福島県立医科大学(福島)     
国立国際医療研究センター(東京) 
明石医療センター(兵庫)
三田市民病院(兵庫)
JR広島病院(広島)
松山赤十字病院(愛媛)
さくら会病院(大阪)
国立病院機構九州医療センター(福岡)
市立札幌病院(北海道)
済生会横浜東部病院 (神奈川)
太田総合病院(福島)
北里大学(神奈川)
鳥取大学(鳥取)
岡崎市民病院(愛知)
天理よろづ病院(奈良)
日本大学(東京)
九州大学病院(福岡)
武蔵野赤十字病院(東京)
JCHO九州病院(福岡)
済生会福岡総合病院(福岡)


Other administrative information

Date of disclosure of the study information

2015 Year 08 Month 25 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

3000

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

No longer recruiting

Date of protocol fixation

2015 Year 05 Month 18 Day

Date of IRB

2015 Year 05 Month 18 Day

Anticipated trial start date

2015 Year 09 Month 01 Day

Last follow-up date

2021 Year 12 Month 01 Day

Date of closure to data entry

2021 Year 12 Month 01 Day

Date trial data considered complete


Date analysis concluded



Other

Other related information

Multicenter, observation study.


Management information

Registered date

2015 Year 08 Month 21 Day

Last modified on

2019 Year 08 Month 26 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000021690


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name