Oral cleft prevention program (OCPP).

dc.contributor.author

Wehby, George L

dc.contributor.author

Goco, Norman

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Moretti-Ferreira, Danilo

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Felix, Temis

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Richieri-Costa, Antonio

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Padovani, Carla

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Queiros, Fernanda

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Guimaraes, Camilla Vila Nova

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Pereira, Rui

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Litavecz, Steve

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Hartwell, Tyler

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Chakraborty, Hrishikesh

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Javois, Lorette

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Murray, Jeffrey C

dc.date.accessioned

2021-01-04T15:09:05Z

dc.date.available

2021-01-04T15:09:05Z

dc.date.issued

2012-11-26

dc.date.updated

2021-01-04T15:09:04Z

dc.description.abstract

Oral clefts are one of the most common birth defects with significant medical, psychosocial, and economic ramifications. Oral clefts have a complex etiology with genetic and environmental risk factors. There are suggestive results for decreased risks of cleft occurrence and recurrence with folic acid supplements taken at preconception and during pregnancy with a stronger evidence for higher than lower doses in preventing recurrence. Yet previous studies have suffered from considerable design limitations particularly non-randomization into treatment. There is also well-documented effectiveness for folic acid in preventing neural tube defect occurrence at 0.4 mg and recurrence with 4 mg. Given the substantial burden of clefting on the individual and the family and the supportive data for the effectiveness of folic acid supplementation as well as its low cost, a randomized clinical trial of the effectiveness of high versus low dose folic acid for prevention of cleft recurrence is warranted.This study will assess the effect of 4 mg and 0.4 mg doses of folic acid, taken on a daily basis during preconception and up to 3 months of pregnancy by women who are at risk of having a child with nonsyndromic cleft lip with/without palate (NSCL/P), on the recurrence of NSCL/P. The total sample will include about 6,000 women (that either have NSCL/P or that have at least one child with NSCL/P) randomly assigned to the 4 mg and the 0.4 mg folic acid study groups. The study will also compare the recurrence rates of NSCL/P in the total sample of subjects, as well as the two study groups (4 mg, 0.4 mg) to that of a historical control group. The study has been approved by IRBs (ethics committees) of all involved sites. Results will be disseminated through publications and presentations at scientific meetings.The costs related to oral clefts are high, including long term psychological and socio-economic effects. This study provides an opportunity for huge savings in not only money but the overall quality of life. This may help establish more specific clinical guidelines for oral cleft prevention so that the intervention can be better tailored for at-risk women. CLINICALTRIALS.GOV IDENTIFIER: NCT00397917.

dc.identifier

1471-2431-12-184

dc.identifier.issn

1471-2431

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1471-2431

dc.identifier.uri

https://hdl.handle.net/10161/21988

dc.language

eng

dc.publisher

Springer Science and Business Media LLC

dc.relation.ispartof

BMC pediatrics

dc.relation.isversionof

10.1186/1471-2431-12-184

dc.subject

Humans

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Cleft Palate

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Cleft Lip

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Folic Acid

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Vitamin B Complex

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Clinical Protocols

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Preconception Care

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Prenatal Care

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Drug Administration Schedule

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Follow-Up Studies

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Pilot Projects

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Double-Blind Method

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Pregnancy

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Dose-Response Relationship, Drug

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Research Design

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Dietary Supplements

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Infant, Newborn

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Female

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Secondary Prevention

dc.title

Oral cleft prevention program (OCPP).

dc.type

Journal article

duke.contributor.orcid

Chakraborty, Hrishikesh|0000-0001-9078-845X

pubs.begin-page

184

pubs.issue

1

pubs.organisational-group

School of Medicine

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Duke Clinical Research Institute

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Biostatistics & Bioinformatics

pubs.organisational-group

Duke

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Basic Science Departments

pubs.publication-status

Published

pubs.volume

12

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