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Neural Tube Defects clinical trials

View clinical trials related to Neural Tube Defects.

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NCT ID: NCT00636233 Completed - Anencephaly Clinical Trials

Genetics of Spina Bifida and Anencephaly

Start date: May 1993
Phase:
Study type: Observational

The goal of this research study is to discover the genetic and environmental factors that contribute to the cause of neural tube defects such as spina bifida and anencephaly. Ultimately, this type of research may result in improved diagnosis, improved treatment and possibly prevention.

NCT ID: NCT00468481 Completed - Contraception Clinical Trials

Efficacy and Safety Study for an Oral Contraceptive Containing Folate

Start date: April 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether the study drug is safe and effective

NCT ID: NCT00452829 Completed - Clinical trials for Recurrent Neural Tube Defects

Prevention of Neural Tube Defects by Inositol in Conjunction With Folic Acid (PONTI Study)

Start date: September 2009
Phase: Phase 1
Study type: Interventional

The aim of the study is to develop a randomised, double blind clinical trial to compare (i) folic acid plus inositol, with (ii) folic acid plus placebo, for prevention of recurrent neural tube defects.

NCT ID: NCT00394862 Completed - Neural Tube Defects Clinical Trials

Efficacy of Weekly Versus Daily Folic Acid Supplementation

Start date: January 2006
Phase: N/A
Study type: Interventional

Investigate the efficacy of weekly versus daily of folic acid supplementation on improving folate, vitamin B12,

NCT ID: NCT00341068 Terminated - Clinical trials for Hereditary Oral Clefts

Genetic Analysis of Neural Tube and Orofacial Cleft Defects in the Irish Population

Start date: January 1, 2000
Phase:
Study type: Observational

In a collaborative effort with the Health Research Board, the national organization for medical research in the Republic of Ireland, individuals with neural tube defects (NTDs) or facial cleft defects and their parents will be studied. With the exception of a few well-described syndromes most cases of NTDs and facial clefts are not inherited in a Mendelian fashion. Nearly all incident cases occur in families with no prior history of the defects. The observed recurrence risk in families with an NTD child is 10-12 fold higher than the general population suggesting that inherited factors modify this risk. Historically, the incidence of NTDs in Ireland was 5-8 fold higher than the USA. The aim of this study is to identify the gene(s) involved in these defects using standard genetic epidemiology approaches, transmission disequilibrium testing and gene mapping strategies. We will initially evaluate genes known to be involved in folate metabolism and pattern formation (development of the body). The major outcomes measured will be aggregate allele frequencies in case groups compared to controls. Biochemical parameters in red cells and plasma will also be measured. Comparisons will be made between the presence of genetics variants, biochemical parameters and clinical phenotype. Characterizing the genes associated with these defects should provide insight into the etiology and metabolic processes that may be involved, furthering prevention and intervention efforts.

NCT ID: NCT00301587 Withdrawn - Neural Tube Defects Clinical Trials

A Study to Evaluate Folate Levels in Women Taking Oral Contraceptives

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare red blood cell folate levels in women who are taking oral contraceptives with or without folic acid

NCT ID: NCT00207558 Completed - Clinical trials for Neural Tube Defects - Spina Bifida and Anencephaly

Blood Folate and Homocysteine Levels Following Administration of Folic Acid According to Different Daily Dosing Schedules:a Simulation of Food Fortification

Start date: n/a
Phase: N/A
Study type: Interventional

The aim of this study is to examine whether the same total daily dosage of folic acid, when taken as a single daily dose or as multiple divided doses throughout the day, results in different blood folate and homocysteine levels at the conclusion of the study. Further, a comparison of blood folate and homocysteine levels among women taking daily low-dosage (100mcg) and standard- dosage (400mcg) folic acid with those of women taking daily or weekly high-dosage (4000mcg) folic acid will be conducted.

NCT ID: NCT00060606 Completed - Spinal Dysraphism Clinical Trials

Management of Myelomeningocele Study (MOMS)

MOMS
Start date: February 2003
Phase: N/A
Study type: Interventional

Spina bifida (myelomeningocele) is a complex birth defect in which a portion of the spinal cord is not fully developed. The overlying bones and skin are incompletely formed and the underdeveloped area of the spinal cord is exposed on the surface of the back. Spina bifida defects are closed soon after birth to prevent further damage to the spinal cord and nerves. The Management of Myelomeningocele Study (MOMS) is a research study comparing two approaches to the treatment of babies with spina bifida: surgery before birth (prenatal surgery) and the standard closure, surgery after birth (postnatal surgery).