Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:46 PM
Ignite Modification Date:
2025-12-24 @ 10:46 PM
NCT ID:
NCT02336269
Eligibility Criteria:
Inclusion Criteria:
* Buccal swab sample prospectively collected under Informed Consent
* Remnant Buccal swab sample meeting the FDA requirements for use of leftover specimen
* Samples from at least one of the following groups:
* specimens from subjects who are on multiple medications of which at least 2 are affected by the pathways tested and the physician made changed to their drug regimen based on the assay interpretations
* subjects who are on multiple medications of which at least 2 are affected by the pathways tested and the physician made no changes based on the assay interpretations
* Subjects with Chronic disease
* Subjects with different ethnic backgrounds
* Subjects from different geographical areas
* Apparently healthy subjects
* Clinical information required per CRF is available
Exclusion Criteria:
\- Samples that do not meet all inclusion criteria
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02336269
Study Brief:
Protocol Section:
NCT02336269