# Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the Treatment of Iris Defects

> **NCT01860612** · NA · UNKNOWN · sponsor: **Clinical Research Consultants, Inc.** · enrollment: 500 (estimated)

## Conditions studied

- Full Aniridia
- Partial Aniridia

## Interventions

- **DEVICE:** Artificial Iris (CustomFlex)

## Key facts

- **NCT ID:** NCT01860612
- **Lead sponsor:** Clinical Research Consultants, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2013-10
- **Primary completion:** 2025-12-31
- **Final completion:** 2025-12-31
- **Target enrollment:** 500 (ESTIMATED)
- **Last updated:** 2022-10-24

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01860612

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01860612, "Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the Treatment of Iris Defects". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01860612. Licensed CC0.

---

*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*