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Generating Advancements Through Longitudinal Analysis in X and Y Variations (GALAXY)
Generating Advancements Through Longitudinal Analysis in X and Y Variations
Who can join
0 Days – 100 Years · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: 1. Genetically-confirmed diagnosis of a sex chromosome aneuploidy condition 2. Any age 3. Any gender 4. Informed consent for individuals \>18 years of age, parent/guardian permission for individuals \<18 or proxy-consent from legally authorized representative if impaired decision making Exclusion Criteria: a. Lack of documentation of genetic testing confirming SCA diagnosis
About the study
GALAXY is a registry research study that plans to learn more about individuals with X\&Y variations (also called sex chromosome aneuploidies) through collecting information from medical records.This includes genetic tests, imaging, medications, and more for hundreds of patients seen at a number of clinics across the US. The purpose of the GALAXY Registry is to collect and store this information with the overall goal to improve health outcomes in individuals with X\&Y variations and the care they receive.
What is being tested
- no intervention (other)
Sponsor: University of Colorado, Denver · Participants: 5,000 · Started: Apr 28, 2022
Contact the study team
- Shanlee M Davis, MD, PhD · Phone: 720-777-6073
Official record on ClinicalTrials.gov — NCT06373861
Locations in the U.S.
| Colorado | Children's Hospital Colorado, Aurora |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.