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临床试验/NCT00397917
NCT00397917已完成3 期

Oral Cleft Prevention Program

University of Iowa1 个研究点 分布在 1 个国家目标入组 4,000 人开始时间: 2006年11月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
4,000
试验地点
1
主要终点
Recurrence of cleft lip and palate

研究概览

简要总结

The purpose of this study is to asses if taking 4 mg of folic acid per day at preconception and during the first three months of pregnancy decreases the risk of having a child with cleft lip and palate compared to 0.4 mg folic acid for women who have an oral cleft or have had previously child with an oral cleft.

详细描述

Cleft lip and palate is a common and burdensome birth defect that has large health ramifications and requires surgical, speech, behavioral, dental, and medical interventions. There is some evidence suggesting that taking folic acid particularly at large doses during preconception and first trimester of pregnancy may decrease the risk of oral cleft recurrence, which is the risk of having a child with an oral cleft for women who have an oral cleft or who have had a child with a cleft. However this evidence is based on study designs that are incapable of contributing the preventive effects to folic acid with adequate confidence, and the real effect of folic acid on cleft recurrence prevention remains to be identified. Taking 4 mg of folic acid per day at preconception and first trimester of pregnancy has also been shown to prevent the recurrence of neural tube defects by up to 70%, providing further support to evaluate this intervention for oral cleft recurrence.

This study evaluates the effects of supplementation with 4 versus 0.4 mg of folic acid per day at preconception and during the first three months of pregnancy on recurrence of cleft lip and palate. Up to 6000 women will be randomly assigned to 4 versus 0.4 mg groups. The primary aim is to compare the recurrence rates in the offspring of trial mothers in the two groups. Secondary aims are to compare the two groups on several outcomes including miscarriage, twinning, pre-eclampsia, serum and red cell folate levels, severity of oral clefts and occurrence of other birth defects in the offspring of trial mothers, and birth weight and gestational age of trial babies, and to compare the recurrence in the two groups to that in historic controls.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Random number assignments

入排标准

年龄范围
16 Years 至 45 Years(Child, Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Women with cleft lip with/out palate (CLP), 16 to 45 years of age registered at the study clinics in Brazil or Women (16 to 45 years of age) with at least one natural child of any age with CLP registered at the study clinics.
  • •Women must reside in the catchment area of the study, which includes the states where the study clinics are located and surrounding states.

排除标准

  • •Consanguineous couples (up to third degree, i.e. first cousins or closer).
  • •Pregnany at the time of recruitment. Women will be recontacted later at an appropriate time for participation in the study.
  • •Couples either one of which have been sterilized.
  • •Taking any form of seizure medication.
  • •Planning to move outside of the study catchment area within the next year.
  • •B12 deficiency (<174 pg/mL or 129.15 pmol/L).
  • •Being allergic to folic acid.

研究组 & 干预措施

400 micrograms of folic acid

Active Comparator

Blinded study with two arms one of 400ug in arm 1

干预措施: Folic acid: 4 mg versus 0.4 mg per day (Drug)

4mg of folic acid

Active Comparator

Second arm is 4mg of folic acid in arm 2

干预措施: Folic acid: 4 mg versus 0.4 mg per day (Drug)

结局指标

主要结局

Recurrence of cleft lip and palate

时间窗: 3 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jeff Murray

Professor of Pediatrics

University of Iowa

研究点 (1)

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