Viewing Study NCT01668251


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Study NCT ID: NCT01668251
Status: UNKNOWN
Last Update Posted: 2012-08-20
First Post: 2011-11-03
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Turner Syndrome Prenatal Diagnosis Study
Sponsor: Seattle Children's Hospital
Organization:

Study Overview

Official Title: National Collaborative Study of Girls Prenatally Diagnosed With Turner Syndrome Karyotypes
Status: UNKNOWN
Status Verified Date: 2012-08
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this study is to compare the features of Turner syndrome in girls who are diagnosed before birth because of fetal concerns versus those who are diagnosed when their mother has an amniocentesis for another reason.
Detailed Description: This is an observational study which will look at girls who are diagnosed with Turner syndrome before they are born. Girls will be divided into two groups: 1) those diagnosed because of features seen on ultrasound which raised the question of Turner syndrome and 2) those diagnosed incidentally when their mother had an amniocentesis for another reason such as advanced maternal age.

No clinical procedures nor interventions will be done as part of this data collection study which will occur for the first 3 to 6 years of the girl's life. The investigators will be looking to see if girls who are diagnosed incidentally have less features of Turner syndrome than those girls who are diagnosed because of fetal ultrasound.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: