Study of Alkaptonuria
Study of Alkaptonuria
Recruiting · NCT00005909 · Registry updated 2026-09-01Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Study of Alkaptonuria | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Nutritional and Metabolic Diseases, Pathologic Processes, Pathological Conditions, Signs and Symptoms, alkaptonuria, arthritic joint disease, arthropathy, hereditary disease, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, musculoskeletal system disorder, ochronosis disorder | Recruiting | Not stated | 2026-09-01 | NCT00005909 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| National Human Genome Research Institute (NHGRI) | 54 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| National Institutes of Health Clinical Center | Bethesda | United States | 800 |