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NCT01253746 Clinical Trial

Genetics of Neural Tube Defects

Neural Tube Defects Clinical Trial

— NTD  

Official title:
Genetics of Neural Tubes Defects

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01253746
Other study ID # 1072
Secondary ID
Status Recruiting
Phase N/A
First received December 2, 2010
Last updated December 2, 2010
Start date April 2009

Study information
Verified date December 2010
Source John P. Hussman Institute for Human Genomics
Contact Maria Ciliberti, MPH
Phone 305-243-4360
Email mciliberti@med.miami.edu
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The Genetics of Neural Tube Defects Study at the University of Miami: The University of Miami John P. Hussman Institute for Human Genomics is looking for families to participate in research to identify the genetic and environmental factors that contribute to Neural Tube Defects (NTD). Our research goal is to better understand the genetic and environmental causes of both open NTD, like spina bifida and anencephaly, and closed NTD, like lipomeningocele and tethered cord. This will eventually lead to more accurate genetic counseling and risk assessment, improved treatments, and better prevention methods. Any individual with a diagnosis of NTD and his/her selected family members can participate, if willing. Participation is free. Travel is not required. Participation involves reading and signing a consent form, providing a blood sample, a family and medical history interview, and granting the research staff permission to review the medical records of the individual(s) with NTD. We maintain the highest standards of confidentiality for all families. If interested, please contact Maria Ciliberti, the study coordinator, at 1-877-686-6444 (toll free) or directly at 305-243-4360, or by email Mciliberti@med.miami.edu . Please visit our web site at www.hihg.org for more information.

Recruitment information / eligibility
Status Recruiting
Enrollment 6000
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria: Any individual with a diagnosis of NTD and his/her selected family members can participate, if willing -

Exclusion Criteria: Pregnant children will not be enrolled

Study Design

Observational Model: Family-Based, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of Miami John P. Hussman Institute for Human Genomics Miami Florida

Sponsors (2)
Lead Sponsor Collaborator
John P. Hussman Institute for Human Genomics University of Miami

Country where clinical trial is conducted

United States, 

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