Genotype and Phenotype Registry: Enrollment of Normal Control Subjects for Current and Future Research

Completed

• Conditions: Healthy

• Registration Number: NCT00926042
• Lead Sponsor: Northwell Health

Brief Summary

Registry program for volunteers who are willing to serve as control subjects in future research studies.

Detailed Description

The registry is a collection of volunteers willing to participate as control subjects in research studies. Control subjects are people who do not have a specific disease; therefore they can serve a critical role as a comparison with people who have the disease or other characteristic being studied. Once registered, participants will be notified about studies they may be able to participate in as a control.

Participation requires:

1. signing a consent form

2. answering a short health survey

3. providing a DNA sample via a mouthwash kit

The registry allows scientists to select study participants based on whether or not they have a specific genetic change that may be relevant to a disease under investigation. Having the ability to access controls when needed is an extremely valuable resource that will speed up scientific discoveries.

Study Timeline

• Study Start: 2004-02
• Study First Submitted: 2009-06-19
• Study First Submitted QC: 2009-06-22
• Study First Posted: 2009-06-23
• Primary Completion: 2012-08
• Study Completion: 2012-08
• Status Verified: 2016-09
• Last Update Submitted: 2016-09-16
• Last Update Posted: 2016-09-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 4511

Inclusion Criteria

• Generally healthy
• over age 18

Exclusion Criteria

• under age 18

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

The Feinstein Institute for Medical Research; 🇺🇸 Manhasset, New York, United States