Use of Partial Body Weight Support Play Environment to Encourage Mobility and Exploration in Infants With Down Syndrome
NCT05307523
Abnormalities, Multiple, Chromosome Disorders
Seattle, Washington, United States
View Trial DetailsNCT Number: NCT00877292
The study will examine the sensitivity and specificity of a circulating cell-free nucleic acid test (DNA/RNA) to identify Down syndrome between about 10 weeks and 21 weeks 6 days gestation. In addition, the new test may be used to identify trisomy 13 and 18 as part of a more complete laboratory developed test. We hypothesize that the new circulating cell-free fetal NA-based test will accurately and precisely measure specific fetal markers in maternal circulation and that measurement will lead to the ability to noninvasively identify with high sensitivity and specificity, fetal chromosome abnormalities, such as Down syndrome.
Looking for future studies?
Notify Me18 year and older
Female
Observational
Center for Medical Education and Clinical Investiagtion, Buenos Aires, Argentina
The RNA study is an observational trial whose primary aim is to document the performance (sensitivity and specificity) of one or more laboratory developed test (LDT) using circulating cell-free fetal nucleic acids from maternal plasma to identify Down syndrome. Multiple test modalities are being pursued, including massively parallel sequencing and those utilizing differential methylation. The population being studied is women already having a diagnostic test (e.g., amniocentesis, CVS) between 10 weeks and 21 weeks 6 days gestation, and whose pregnancy is at high risk for having Down syndrome. The women provide informed consent. The karyotype will provide the gold standard against which the LDT test is judged. Samples and karyotypes will be collected from up to 25 prenatal diagnostic centers around the world and tested in several laboratories in the United States. The secondary aim is to develop a nucleic acid sample bank to allow documentation of subsequent improvements or new methodologies to identify fetal aneuploidy using circulating cell-free fetal nucleic acids.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Within 1st and 2nd trimesters
Time frame: Late1st and early 2nd trimesters
Women and Infants Hospital of Rhode Island
Other
The RNA (RNA-Based Noninvasive Aneuploidy) Study
Acronym: RNA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05307523
Abnormalities, Multiple, Chromosome Disorders
Seattle, Washington, United States
View Trial DetailsNCT02201862
Abnormalities, Multiple, Aneuploidy
San Diego, California, United States
View Trial DetailsNCT01821300
Abnormalities, Multiple, Body Weight
Washington D.C., District of Columbia, United States
View Trial DetailsNCT05527652
Abnormalities, Multiple, Airway Obstruction
Ann Arbor, Michigan, United States
View Trial Details