# Clinical Study to Evaluate Clinical Outcomes of LuxSmart IOL as Compared With LuxGood IOL

> **NCT06105190** · NA · ACTIVE_NOT_RECRUITING · sponsor: **Cutting Edge SAS** · enrollment: 251 (actual)

## Conditions studied

- Cataract
- Lens Opacities

## Interventions

- **DEVICE:** Implantation of premium monofocal IOL, LuxSmart (device under investigation)
- **DEVICE:** Implantation of monofocal IOL, LuxGood (control device)

## Key facts

- **NCT ID:** NCT06105190
- **Lead sponsor:** Cutting Edge SAS
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** ACTIVE_NOT_RECRUITING
- **Start date:** 2023-06-21
- **Primary completion:** 2025-04
- **Final completion:** 2025-04
- **Target enrollment:** 251 (ACTUAL)
- **Last updated:** 2025-02-12

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06105190

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06105190, "Clinical Study to Evaluate Clinical Outcomes of LuxSmart IOL as Compared With LuxGood IOL". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT06105190. Licensed CC0.

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