Kidney Information Network for Disease Research and Education
NCT03321604 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 338
Last updated 2021-02-24
Summary
In this study, Investigators will conduct a prospective cohort study of dialysis patients by collecting research-quality information on patient characteristics, comorbid diseases and laboratory markers used in routine practice, as well as novel biochemical markers and genetic data. Investigators will utilize data from the cohort to test the independent relationship between biochemical and genetic markers and Fabry disease and other rare diseases.
Conditions
- ESRD
- Fabry Disease
- Rare Diseases
- Kidney Diseases
- End Stage Renal Disease
- Genetic Diseases, X-Linked
Sponsors & Collaborators
-
Genzyme, a Sanofi Company
collaborator INDUSTRY -
Scott and White Hospital & Clinic
collaborator OTHER -
Massachusetts General Hospital
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-01-01
- Primary Completion
- 2019-11-21
- Completion
- 2019-11-21
Countries
- United States
Study Locations
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