Trials / Completed
CompletedNCT00098319
Oral Cleft Prevention Trial in Brazil
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 2,200 (estimated)
- Sponsor
- NICHD Global Network for Women's and Children's Health · Network
- Sex
- Female
- Age
- 16 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
Cleft lip and palate are a significant component of morbid human birth defects in the developing world. By supplementing a high-risk group of women with folic acid (4.0 mg versus 0.4 mg) from preconception and continuing throughout the first 3 months of pregnancy in the state of Sao Paulo, Brazil, this study aims to reduce the recurrence of cleft lip and palate.
Detailed description
Craniofacial anomalies and cleft lip with or without cleft palate (CL/P) are a model for the impact of birth defects on fetal and neonatal health directly and maternal health indirectly. Craniofacial anomalies comprise a significant component of morbid human birth defects. The primary hypothesis is that folic acid supplementation of 4mg/day at preconception and during the first three months of pregnancy will decrease the recurrence of nonsyndromic cleft lip with or without clef palate (NSCL/P) in a high-risk group of women when compared to women taking 0.4 mg per day of folic acid. The total sample will include 2,000 women (that either have NSCL/P or that have at least one child with NSCL/P) randomly assigned to the 4 mg versus 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 (4mg, 0.4 mg) to that of a historical control group. The primary outcome assessed is the rate of recurrences of NSCL/P in offspring of the trial mothers in each of the two study groups. Secondary outcomes include recurrence of NSCL/P compared to a historical control group; serum and red cell folate levels; severity of NSCL/P in offspring of trial mothers; twinning rate; miscarriage rate; preeclampsia; rates of other birth defects; birth weight; and gestational age. The sample size was based on historic tables of birth rates and the rates of cleft occurrences. The study hypothesizes that a total of 2000 subjects will be enrolled during a 2.5 year period; a dropout rate of 10%; birth rate for group A (women with NSCL/P) of 10% and a rate of 12% for group B (women with at least one child with NSCL/P); risk of cleft for group A is 7% and for group B is 4%; one-sided test with continuity correction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Folic acid (0.4mg vs. 4.0mg) |
Timeline
- Start date
- 2004-01-01
- Completion
- 2007-04-01
- First posted
- 2004-12-07
- Last updated
- 2013-12-17
Locations
3 sites across 1 country: Brazil
Source: ClinicalTrials.gov record NCT00098319. Inclusion in this directory is not an endorsement.