Clinical trial
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive…
NCT00494169 · Massachusetts General Hospital, Other · Completed
Key facts
| NCT number | NCT00494169 |
|---|---|
| Title | Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders |
| Official title | Molecular Basis of Inherited Reproductive Disorders |
| Lead sponsor | Massachusetts General Hospital, Other |
| Status | Completed |
| Study type | Observational |
| Conditions | Hypogonadotropic Hypogonadism, Kallmann Syndrome, Puberty, Delayed, Precocious, GnRH Deficiency |
| Enrollment | 4,042 |
| Start date | Jan 1, 1999 |
| Primary completion | Feb 1, 2022 |
| Completion | Feb 1, 2022 |
| First posted | Jun 29, 2007 |
| Last update posted | Jun 30, 2022 |
| 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.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: