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Systematic Pediatric Care for Oral Clefts - South America

Systematic Pediatric Care for Oral Clefts - South America

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00097149
Enrollment
696
Registered
2004-11-18
Start date
2003-05-31
Completion date
2006-05-31
Last updated
2013-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cleft Lip, Cleft Palate, Congenital Defects

Keywords

Congenital birth defects, Cleft lip, Cleft palate, Global Network, Neurodevelopmental outcome, Maternal and child health, International, Women's health, Brazil, Brasil, Latin America, ECLAMC, Argentina, Bolivia, Chile, Colombia, Ecuador, Venezuela

Brief summary

Cleft lip and palate are a significant component of morbid human birth defects in the developing world. This study measures the impact of having a child born with a cleft lip on subsequent maternal/infant family health, and whether frequent pediatric care compared to standard pediatric care will reduce neonatal mortality in children born with 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. This study is composed of two Subprojects, A and B. Subproject A involves provision of intensive pediatric care over the first 28 days of life for a prospective group of about 694 cleft cases, which will be compared to a retrospective group of about 464 cleft cases. Nonsyndromic cleft lip with or without cleft palate (NSCL/P) cases (about 264 cases) of Subproject A will be randomized into two groups: intervened (about 132 cases) and non-intervened (about 132 cases). Sub-project B involves provision of systematic pediatric care over a 2-year period for the intervened group. This group will be compared to the non-intervened group in order to study the effect of the intervention on the neurodevelopment and physical health of the child as well as the emotional and social health of the family. The standard care group also will be compared to a group of about 264 healthy controls, matched by sex and place and date of birth in order to study the impact of the cleft on the physical health and neurodevelopment of the child as well as the emotional and social health of the family. The importance of the study relates to the substantial burden caused by clefts and the necessity of developing and testing approaches that may lessen this burden. The outcomes of this project will be to further strengthen collaborative relationships in the area of craniofacial anomalies between South America and the United States; to better understand the effects of birth defects, and craniofacial anomalies in particular, on maternal family units; and, to decrease the burden of these defects directly. The sample size was based on an expected overall 28 days mortality rate among cleft infants that is around 0.25, calculated at a 0.05 significance level.

Interventions

PROCEDURESystematic pediatric care

Sponsors

Global Network for Women's and Children's Health Research
CollaboratorOTHER
Bill and Melinda Gates Foundation
CollaboratorOTHER
National Institute of Dental and Craniofacial Research (NIDCR)
CollaboratorNIH
Fogarty International Center of the National Institute of Health
CollaboratorNIH
National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
National Cancer Institute (NCI)
CollaboratorNIH
RTI International
CollaboratorOTHER
University of Iowa
CollaboratorOTHER
Latin-American Collaborative Study of Congenital Malformations (ECLAMC)
CollaboratorOTHER
NICHD Global Network for Women's and Children's Health
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 2 Years
Healthy volunteers
No

Inclusion criteria

Subproject A: * All children born with an oral cleft in a participating hospital (hospitals in Argentina, Bolivia, Brazil, Chile, Colombia and Venezuela affiliated with ECLAMC) Subproject B: Cases from Subproject A that meet the following criteria: * Cleft lip with or without cleft palate or cleft palate only * Birth weight \>2500 g * No other identifiable birth defect: nonsyndromic * Singleton (nonmultiple birth) * No other complications requiring systematic care

Design outcomes

Primary

MeasureTime frame
SUBPROJECT A: Neonatal mortality
SUBPROJECT B: Neurodevelopmental outcome
Weight

Secondary

MeasureTime frame
SUBPROJECT A: Hospitalizations, Weight
SUBPROJECT B: Height, Speech, Hearing, Mortality, Cleft surgery, Rate of weight gain, Financial burden, Syndromic classification, Emotional and social family development

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026