Clinical trial
Clinical and Genetic Studies on Holoprosencephaly
NCT00088426 · National Human Genome Research Institute (NHGRI), NIH · Completed
Key facts
| NCT number | NCT00088426 |
|---|---|
| Title | Clinical and Genetic Studies on Holoprosencephaly |
| Official title | Clinical and Genetic Studies on Holoprosencephaly |
| Lead sponsor | National Human Genome Research Institute (NHGRI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Holoprosencephaly, HPE, Developmental Delay Disorders, Brain Disorders |
| Enrollment | 256 |
| Start date | Jan 23, 2004 |
| Primary completion | Mar 16, 2020 |
| Completion | Apr 16, 2020 |
| First posted | Jul 26, 2004 |
| Last update posted | Apr 20, 2020 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About ClinicalTrials.gov studies
ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.
Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: