Viewing StudyNCT00031122



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Last Modification Date: 2024-10-26 @ 9:07 AM
Study NCT ID: NCT00031122
Status: UNKNOWN
Last Update Posted: 2010-10-05
First Post: 2002-02-26

Brief Title: Study of Genetic Risk Factors for Spina Bifida and Anencephaly
Sponsor:
Organization: Office of Rare Diseases ORD

Study Design

Study Type: OBSERVATIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: SAMPLES_WITH_DNA
Bio Spec Description: DNA extracted from whole blood saliva buccal swab andor amniocytes
Enrollment Count: 1100
Enrollment Type: ESTIMATED
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
Name
Family-Based
Time Perspective List:

Clinical Trial Statuses

Name
359
Who Masked List: