UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000042782
Receipt number R000048703
Scientific Title Prospective registry study of primary dyslipidemia
Date of disclosure of the study information 2020/12/20
Last modified on 2020/12/18 18:53:10

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Basic information

Public title

Prospective registry study of primary dyslipidemia

Acronym

PROLIPID

Scientific Title

Prospective registry study of primary dyslipidemia

Scientific Title:Acronym

PROLIPID

Region

Japan


Condition

Condition

Homozygous familial hypercholesterolemia (homo-FH)
Heterozygous familial hypercholesterolemia (hetero-FH)
Type III Hyperlipoproteinemia
Familial chylomicronemia
Sitosterolemia
Cerebrotendinous xanthomatosis
Lecithin cholesterol acyltransferase (LCAT) deficiency
Tangier disease
Abetalipoproteinemia

Classification by specialty

Endocrinology and Metabolism

Classification by malignancy

Others

Genomic information

YES


Objectives

Narrative objectives1

The objectives of this registry are to describe natural cause and clinical practice including treatment of primary dyslipidemia, and to provide reliable information on the type of practice performed and the prognosis of patients in Japan.

Basic objectives2

Others

Basic objectives -Others

Patient Registry

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Incidence of adverse outcomes in patients with primary dyslipidemia
[Through study completion]

Key secondary outcomes

All-cause mortality
[Through study completion]


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Clinical and/or genetic diagnosis of the following Primary dyslipidemia:
Homozygous familial hypercholesterolemia (homo-FH)
Heterozygous familial hypercholesterolemia (hetero-FH)
Type III Hyperlipoproteinemia
Familial chylomicronemia
Sitosterolemia
Cerebrotendinous xanthomatosis
Lecithin cholesterol acyltransferase (LCAT) deficiency
Tangier disease
Abetalipoproteinemia

Key exclusion criteria

Patients who refused to consent

Target sample size

1000


Research contact person

Name of lead principal investigator

1st name Mariko
Middle name
Last name Shiba

Organization

National Cerebral and Cardiovascular Center

Division name

Department of Molecular Pathogenesis

Zip code

564-8565

Address

6-1 Kishibeshin-machi, Suita, Osaka

TEL

06-6170-1070

Email

mshiba@ncvc.go.jp


Public contact

Name of contact person

1st name Masatsune
Middle name
Last name Ogura

Organization

National Cerebral and Cardiovascular Center

Division name

Department of Molecular Innovation in Lipidology

Zip code

564-8565

Address

6-1 Kishibeshin-machi, Suita, Osaka

TEL

06-6170-1070

Homepage URL

https://nanbyo-lipid.com/prolipid/

Email

enustasam@ncvc.go.jp


Sponsor or person

Institute

National Cerebral and Cardiovascular Center

Institute

Department

Personal name



Funding Source

Organization

Ministry of Health, Labor and Welfare of Japan

Organization

Division

Category of Funding Organization

Japanese Governmental office

Nationality of Funding Organization

Japan


Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

National Cerebral and Cardiovascular Center

Address

6-1 Kishibeshin-machi, Suita, Osaka

Tel

06-6170-1070

Email

rec-office-ac@ncvc.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



Other administrative information

Date of disclosure of the study information

2020 Year 12 Month 20 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

2015 Year 01 Month 21 Day

Date of IRB

2015 Year 02 Month 03 Day

Anticipated trial start date

2015 Year 08 Month 01 Day

Last follow-up date

2023 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This study started at August 1, 2015.


Management information

Registered date

2020 Year 12 Month 18 Day

Last modified on

2020 Year 12 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000048703


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name