Clinical trial
Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the…
NCT01860612 · Clinical Research Consultants, Inc., Industry · Unknown status
Key facts
| NCT number | NCT01860612 |
|---|---|
| Title | Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the Treatment of Iris Defects |
| Official title | Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the Treatment of Iris Defects |
| Lead sponsor | Clinical Research Consultants, Inc., Industry |
| Collaborators | HumanOptics AG Industry |
| Status | Unknown status |
| Study type | Interventional |
| Conditions | Full Aniridia, Partial Aniridia |
| Intervention type | Device |
| Interventions | Artificial Iris (CustomFlex) |
| Enrollment | 500 |
| Start date | Oct 1, 2013 |
| Primary completion | Dec 31, 2025 |
| Completion | Dec 31, 2025 |
| First posted | May 23, 2013 |
| Last update posted | Oct 24, 2022 |
| Countries | United States |
At a glance
- 10–99 Study sites
- No Results posted
- 1–9 FDA inspections linked to this trial
- 1–9 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: