UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000001306
Receipt number R000001583
Scientific Title Double blined rondmised control trial of the effect of folate preventing miscarriage in unexplained recurrent miscarriages.
Date of disclosure of the study information 2008/08/08
Last modified on 2014/05/30 14:56:04

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Basic information

Public title

Double blined rondmised control trial of the effect of folate preventing miscarriage in unexplained recurrent miscarriages.

Acronym

RCT of folate in recurrent miscarriage

Scientific Title

Double blined rondmised control trial of the effect of folate preventing miscarriage in unexplained recurrent miscarriages.

Scientific Title:Acronym

RCT of folate in recurrent miscarriage

Region

Japan


Condition

Condition

unexplained recurrent miscarriage

Classification by specialty

Obstetrics and Gynecology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

to study whethre folate supplementation can prevent further miscarriage in recurrnt miscarriage patients

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Phase I


Assessment

Primary outcomes

live birth rate

Key secondary outcomes

folate level before pregnancy


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Medicine

Interventions/Control_1

folate 5mg

Interventions/Control_2

placebo

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


Not applicable

Gender

Female

Key inclusion criteria

patients without explained causes of recurrent miscarriage

Key exclusion criteria

abnormal chromosome in either partner, congenital uterine anomaly, antiphospholipid antibody
patients with complications who are treated with drugs
patients who have any supplement

Target sample size

200


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Mayumi Sugiura

Organization

Nagoya City University Hospital

Division name

Obstetrics and Gynecology

Zip code


Address

Kawasumi 1, Mizuho-ku, Nagoya, Aichi

TEL

052-851-5511

Email

og.mym@med.nagoya-cu.ac.jp


Public contact

Name of contact person

1st name
Middle name
Last name Mayumi Sugiura

Organization

Nagoya City University Medical School

Division name

Obstetrics and Gunecology

Zip code


Address

Kawasumi 1, Mizuho-ku, Nagoya

TEL

052-851-5511

Homepage URL


Email

og.mym@med.nagoya-cu.ac.jp


Sponsor or person

Institute

Nagoya City University

Institute

Department

Personal name



Funding Source

Organization

Ministry of Health, Labor and Wealfare

Organization

Division

Category of Funding Organization

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

名古屋市立大学病院


Other administrative information

Date of disclosure of the study information

2008 Year 08 Month 08 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

2007 Year 12 Month 11 Day

Date of IRB


Anticipated trial start date

2008 Year 04 Month 01 Day

Last follow-up date

2015 Year 03 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2008 Year 08 Month 08 Day

Last modified on

2014 Year 05 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000001583


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name