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NCT00341133 · ClinicalTrials.gov registry record

Genetic Analysis of Left-Right Axis Formations

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

Completed
Registry status
900
Enrollment target

NCT00341133: Completed study, sponsored by National Human Genome Research Institute (NHGRI).

NCT00341133 is a clinical trial that has completed, run by National Human Genome Research Institute (NHGRI). The registered enrollment target is 900 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00341133 has completed, sponsored by National Human Genome Research Institute (NHGRI).

COMPLETED
Registry status
900 participants
Enrollment target

Study Summary

The objective of these studies is to identify genetic factors that contribute to the pathogenesis of complex congenital heart disease and other more rare conditions resulting from disturbances in organ positioning. These are a group of medical conditions that are thought to stem from a poorly understood disturbance in the establishment of the basic body plan in the embryo. While the outside of the human body is generally symmetric with mirror image left and right sides, the positions of some internal organs are distinctly asymmetric. For example, the heart could not function properly as a mechanical pump if its connections to major blood vessels retained their initial symmetry. The left ventricle of the heart normally pumps blood to the body, while the right ventricle normally pumps blood to the lungs. Reversals in these blood vessel connections can be fatal. Similarly, the gut characteristically loops in a counterclockwise direction placing the stomach on the left side in most cases. Rare laterality anomalies can occur if this looping is in the other direction, or randomized (equally likely to loop in either direction). Serious medical problems can be caused by disturbances in the establishment, or maintenance of left-right (L-R) differences as key organs are developing in the embryo. We have established formal collaborative agreements with three major centers who have collected a large number of coded cases of congenital cardiac disease. Our research objective is to try to understand if specific genetic changes can contribute to a range of cardiac malformations. We utilize mutational analysis of candidate genes as our principal tool to study the genetics of L-R axis malformations. This protocol is also open to other conditions whose basis is also thought to result from L-R problems. In all cases, the patients continue under the care of the referring physician. We anticipate a minor role of NIH researchers and genetic counseling services if subjects either do not

Trial Details

FieldValue
Enrollment Target 900 participants
Start Date 1999-12-13

What the finished NCT00341133 record still lists

NCT00341133 is an observational study that tracks outcomes without assigning an intervention. The registered 900 participants enrollment target is mid-sized for trials with a published cap.

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

NCT00341133 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00341133 about?

NCT00341133 is a clinical study titled "Genetic Analysis of Left-Right Axis Formations". The objective of these studies is to identify genetic factors that contribute to the pathogenesis of complex congenital heart disease and other more rare conditions resulting from disturbances in organ positioning. These are a group of medical conditions that are thought to stem from a poorly unders...

What is the current status of trial NCT00341133?

This trial is currently completed. The enrollment target is 900 participants. The study started on 1999-12-13.

Who is sponsoring clinical trial NCT00341133?

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 NCT00341133, the US trial registry maintained by the National Library of Medicine. NCT00341133 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.