UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000018102
Receipt number R000020950
Scientific Title Effect of plasmalogen-containing food on patients with Parkinson's disease or Parkinsonian syndromes -an open trial-
Date of disclosure of the study information 2015/06/26
Last modified on 2016/06/27 17:51:25

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Basic information

Public title

Effect of plasmalogen-containing food on patients with Parkinson's disease or Parkinsonian syndromes -an open trial-

Acronym

Effect of plasmalogen-containing food on patients with Parkinson's disease or Parkinsonian syndromes

Scientific Title

Effect of plasmalogen-containing food on patients with Parkinson's disease or Parkinsonian syndromes -an open trial-

Scientific Title:Acronym

Effect of plasmalogen-containing food on patients with Parkinson's disease or Parkinsonian syndromes

Region

Japan


Condition

Condition

Parkinson's disease, Parkinsonian syndrome

Classification by specialty

Neurology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the effects on the improvement in symptoms and the plasmalogen hemodynamic alteration by 6-month administration of plasmalogen-containing food

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

UPDRS

Key secondary outcomes

1) H&Y
2) Schwab & England
3) PDQ-39


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

To administer the test food containing 0.5 mg of plasmalogen twice a day for 6 months and observe the changes of UPDRS and other medical indices

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

1. Informed consents are obtained in writing from patients or one of their caretakers
2. Those who regularly go to hospitals conducting this study (regardless of gender)
3. Those who are judged as suitable for participation in this study by responsible doctors at the beginning of the study

Key exclusion criteria

1. Those who have scallop allergy
2. Those who are judged as not suitable for participation in this study by responsible doctors at the beginning of the study

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Shinji Ohara

Organization

BOOCS clinic Fukuoka

Division name

Functional neurology

Zip code


Address

6-18 Tenya-machi, Hakata-ku, Fukuoka city

TEL

092-283-6852

Email

fukuoka@boocsclinic.com


Public contact

Name of contact person

1st name
Middle name
Last name Etsuko Kifuji

Organization

BOOCS clinic Fukuoka

Division name

director of nursing

Zip code


Address

6-18 Tenya-machi, Hakata-ku, Fukuoka city

TEL

092-283-6852

Homepage URL


Email

kifuji@boocsclinic.com


Sponsor or person

Institute

BOOCS clinic Fukuoka

Institute

Department

Personal name



Funding Source

Organization

Plasmalogen Society

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2015 Year 06 Month 26 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

Completed

Date of protocol fixation

2015 Year 05 Month 21 Day

Date of IRB


Anticipated trial start date

2015 Year 06 Month 27 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 06 Month 26 Day

Last modified on

2016 Year 06 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000020950