Clinical trial
Gene Mutations and Orthopaedic Symptoms Correlation of Multiple Hereditary…
NCT00474331 · University of British Columbia, Other · Suspended
Key facts
| NCT number | NCT00474331 |
|---|---|
| Title | Gene Mutations and Orthopaedic Symptoms Correlation of Multiple Hereditary Exostoses: Multicentre Project |
| Official title | Genotype-Phenotype Correlation of Multiple Hereditary Exostoses: Multicentre Project |
| Lead sponsor | University of British Columbia, Other |
| Status | Suspended |
| Study type | Observational |
| Conditions | Exostoses, Multiple Hereditary |
| Enrollment | 2,000 |
| Start date | Jun 1, 2004 |
| Primary completion | Jun 1, 2023 |
| Completion | Jun 1, 2023 |
| First posted | May 16, 2007 |
| Last update posted | May 18, 2022 |
| Countries | Canada |
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: