CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 372 enrolled
Drug / intervention
Bausch & Lomb DVisc40 +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03511638
NCT03511638N/ACompleted

A Study to Document the Safety and Effectiveness of a New OVD When Compared to a Control OVD

Bausch & Lomb Incorporated·interventional·Posted Apr 30, 2018·Updated Oct 22, 2021

In Brief

A clinical study evaluating Bausch & Lomb DVisc40 and Alcon VISCOAT® for Cataract. Completed, enrolled 372 participants across 1 site.

Detailed Summary

A Study to Document the Safety and Effectiveness of a New OVD When Compared to a Control OVD

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCataract
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedApr 30, 2018
Enrollment StartMay 9, 2018
Primary CompletionApr 1, 2019
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 8.2 years ago

Interventions

Bausch & Lomb DVisc40device

Ophthalmic viscosurgical device

Alcon VISCOAT®device

Ophthalmic viscosurgical device