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

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Northwell Health

Status

Completed

Conditions

Healthy

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Full 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.

Enrollment

4,511 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Generally healthy
  • over age 18

Exclusion criteria

  • under age 18

Trial design

4,511 participants in 1 patient group

Healthy Control
Description:
Healthy control group for research on autoimmune diseases

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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