# A Clinical Study Comparing the Comfort of Three Commercially Available Contact Lenses

> **NCT02298400** · NA · WITHDRAWN · sponsor: **ORA, Inc.**

## Conditions studied

- Contact Lens Complication

## Interventions

- **DEVICE:** Acuvue® Oasys® Lenses (senofilcon A)
- **DEVICE:** 30-Day Bausch + Lomb PureVision (balafilcon A)
- **DEVICE:** Clariti® 1-Day (Somofilcon A)

## Key facts

- **NCT ID:** NCT02298400
- **Lead sponsor:** ORA, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** WITHDRAWN
- **Start date:** 2014-08
- **Primary completion:** 2014-09
- **Final completion:** 2014-09
- **Target enrollment:** 0 (ACTUAL)
- **Why stopped:** Study terminated by Sponsor
- **Last updated:** 2024-04-25


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02298400

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02298400, "A Clinical Study Comparing the Comfort of Three Commercially Available Contact Lenses". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT02298400. Licensed CC0.

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