UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000008844
Receipt number R000010208
Scientific Title Evaluation of clinical guideline and establishment of evidence for the diagnosis and treatment of primary hyperaldosteronism in Japan.
Date of disclosure of the study information 2012/09/05
Last modified on 2019/03/11 10:09:56

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Basic information

Public title

Evaluation of clinical guideline and establishment of evidence for the diagnosis and treatment of primary hyperaldosteronism in Japan.

Acronym

PHAS-J3

Scientific Title

Evaluation of clinical guideline and establishment of evidence for the diagnosis and treatment of primary hyperaldosteronism in Japan.

Scientific Title:Acronym

PHAS-J3

Region

Japan


Condition

Condition

Primary aldosteronism

Classification by specialty

Medicine in general Cardiology Endocrinology and Metabolism
Nephrology Neurology Endocrine surgery
Urology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Adherence of clinical guideline and establishment of standard medication of primary adlosteronism

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase IV


Assessment

Primary outcomes

1)Adherance of clinical guideline for PA
2)Establishment of standard medication in PA and Aldosterone-rerated hypertension.

Key secondary outcomes

1)Implementation rate of each diagnostic procedure
2)Successful rate of the localization
3) Comparison of the effects of medical treatments and surgical treatment


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -no one is blinded

Control

Active

Stratification


Dynamic allocation

YES

Institution consideration

Institution is considered as adjustment factor in dynamic allocation.

Blocking

NO

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

Conventional antihypertensive agents with aldosterone antagonist

Interventions/Control_2

Conventional antihypertensive agents

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

Hypertensive patients in the outpatient clinics and hospitals, who full-fill the following 1) or 2) criteria:
1)treated hypertensive patients
2)untreated hypertensive patients with systolic blood pressure higher than 140mmHg or diastolic blood pressure higher than 90mmHg according to the guideline of the Japan Society of Hypertension

Key exclusion criteria

1)pregnant patients
2)patients taking aldosterone antagonist within the last one month
3)patients with the following diseases:
(1)secondary hypertension (renal hypertension,renovascular hypertension, primary aldosteronism, Cushing's syndrome, pheochromocytoma, etc)
(2)patients whom the attending doctors decides not suitable for the entry because of the unstable stage of the following complications: coronary diseases, arrhythmia, severe valvular diseases, cerebrovascular diseases, acute and chronic renal failure (serum Cr higher than 3mg/dl), acute and chronic liver diseases
4) Patients whom the attending doctor decides not suitable for the entry of the study.

Target sample size

2700


Research contact person

Name of lead principal investigator

1st name Mitsuhide
Middle name
Last name Naruse

Organization

National Hospital Organization, Kyoto Medical Center

Division name

Clinical Research Institute for Endocrine and Metabolic Diseases

Zip code

612-8555

Address

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

TEL

075-641-9161

Email

yawata.rinshokenkyubu@gmail.com


Public contact

Name of contact person

1st name Mitsuhide
Middle name
Last name Naruse

Organization

National Hospital Organization, Kyoto Medical Center

Division name

Clinical Research Institute for Endocrine and Metabolic Diseases

Zip code

6128555

Address

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

TEL

075-641-9161

Homepage URL


Email

yawata.rinshokenkyubu@gmail.com


Sponsor or person

Institute

National Hospital Organization

Institute

Department

Personal name



Funding Source

Organization

National Hospital Organization

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor

The Japan Endocrine Society

Name of secondary funder(s)

non


IRB Contact (For public release)

Organization

National Hospital Organization

Address

5-21,2, higashigaoka, meguro-ku, Tokyo, Japan

Tel

03-5712-5075

Email

kenkyu2004@nho.hosp.go.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

NHO函館病院(北海道)、NHO西群馬病院(群馬県)、NHO埼玉病院(埼玉県)、NHO金沢医療センター(石川県)、NHO名古屋医療センター(愛知県)、NHO三重病院(三重県)、NHO三重中央医療センター(三重県)、NHO京都医療センター(京都府)、NHO神戸医療センター(兵庫県)、NHO岡山医療センター(岡山県)、NHO呉医療センター・中国がんセンター(広島県)、NHO小倉医療センター(福岡県)、NHO九州医療センター(福岡県)、NHO長崎川棚医療センター(長崎県)、NHO熊本医療センター(熊本県)、佐世保市立総合病院(長崎県)、みさと健和病院(埼玉県)、岡崎市民病院(愛知県)、伊勢赤十字病院(三重県)


Other administrative information

Date of disclosure of the study information

2012 Year 09 Month 05 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

2641

Results


Results date posted


Results Delayed

Delay expected

Results Delay Reason

on analysis

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

Completed

Date of protocol fixation

2012 Year 07 Month 14 Day

Date of IRB

2012 Year 09 Month 01 Day

Anticipated trial start date

2012 Year 09 Month 01 Day

Last follow-up date

2017 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2012 Year 09 Month 04 Day

Last modified on

2019 Year 03 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000010208


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name