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NCT01952171 · ClinicalTrials.gov registry record

The Genetic Basis of Congenital Heart Disease in Africa

A clinical trial, sponsored by National Human Genome Research Institute (NHGRI).

Completed
Registry status
1,233
Enrollment target

NCT01952171: Completed study, sponsored by National Human Genome Research Institute (NHGRI).

NCT01952171 is a clinical trial that has completed, run by National Human Genome Research Institute (NHGRI). The registered enrollment target is 1,233 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01952171 has completed, sponsored by National Human Genome Research Institute (NHGRI).

COMPLETED
Registry status
1,233 participants
Enrollment target

Study Summary

Recent advances in genomic techniques are making possible a new wave of genetic discovery in congenital heart disease (CHD). Existing data suggests that CHD occur in Sub-Saharan Africa at frequencies similar to the rest of the world. In this application, we propose to utilize the unique advantages of Sub-Saharan Africa - a combination of the most genetically diverse populations in the world and of diminished environmental background effects (i.e. low prevalence of smoking, alcohol abuse, obesity in comparison to western countries) - to better understand the genetic basis for congenital heart disease. We will couple next generation genomic techniques with more traditional gene discovery methods to investigate CHD in two African countries: Uganda and Nigeria. The inclusion of syndromic and non-syndromic CHD observed in these populations as well as careful phenotyping (including echocardiography) will greatly enhance our potential to provide insight into the genetic architecture of CHD in African populations. To accomplish this, we plan to enroll families, in whom members have congenital heart malformations consistent with an error of early human development in our research protocol. Patients will be enrolled at the Uganda Heart Institute in Kampala, Uganda, and at the Department of Pediatrics, College of Medicine, University of Lagos, Nigeria, with the potential to include other African sites. High throughput genomic studies will be done at the NIH.

Primary Outcome

The primary outcome is a genetic diagnosis for congenital heart disease. There are no treatments.

Trial Details

FieldValue
Enrollment Target 1,233 participants
Start Date 2013-09-17

What the finished NCT01952171 record still lists

NCT01952171 is an observational study that tracks outcomes without assigning an intervention. Its 1,233 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 0 interventions.

NCT01952171 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01952171 about?

NCT01952171 is a clinical study titled "The Genetic Basis of Congenital Heart Disease in Africa". Recent advances in genomic techniques are making possible a new wave of genetic discovery in congenital heart disease (CHD). Existing data suggests that CHD occur in Sub-Saharan Africa at frequencies similar to the rest of the world. In this application, we propose to utilize the unique advantages o...

What is the current status of trial NCT01952171?

This trial is currently completed. The enrollment target is 1,233 participants. The study started on 2013-09-17.

Who is sponsoring clinical trial NCT01952171?

This trial is sponsored by National Human Genome Research Institute (NHGRI), which has 185 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01952171, the US trial registry maintained by the National Library of Medicine. NCT01952171 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.