Clinical and Basic Investigations Into Congenital Disorders of Glycosylation
Recruiting now
Conditions studied: Congenital Disorders of Glycosylation
In brief
The purpose of this research is to study the natural history of congenital disorders of glycosylation and its causes and treatments.
Key facts
- Study ID
- NCT04199000
- Run by
- Icahn School of Medicine at Mount Sinai
- People needed
- 500
- Starts
- 2019-10-08
- Expected to finish
- 2030-07-31
- Last updated by the study team
- 2026-07-21
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Individuals with a genetically, enzymatically, or molecularly confirmed diagnosis of CDG or NGLY1 deficiency
You may not qualify if…
- None
Where it is running
- Seattle Children's Hospital — Seattle, Washington, United States (enrolling)
- Children's Hospital of Colorado — Aurora, Colorado, United States (enrolling)
- Mayo Clinic Florida — Jacksonville, Florida, United States (enrolling)
- Rady Children's Hospital — San Diego, California, United States (enrolling)
- Boston Children's Hospital — Boston, Massachusetts, United States (enrolling)
- University of Minnesota — Minneapolis, Minnesota, United States (enrolling)
- Mayo Clinic in Rochester — Rochester, Minnesota, United States (enrolling)
- Icahn School of Medicine at Mount Sinai — New York, New York, United States (enrolling)
- Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States (enrolling)
- Children's Hospital of Pittsburgh — Pittsburgh, Pennsylvania, United States (enrolling)
- Baylor College of Medicine — Houston, Texas, United States (enrolling)
- Tulane University School of Medicine — New Orleans, Louisiana, United States
Full record on ClinicalTrials.gov
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