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NCT03500198 · ClinicalTrials.gov registry record · NA

Clinical Investigation of the Next Generation Intraocular Lens

A NA study, sponsored by Johnson & Johnson Surgical Vision.

Completed
Registry status
NA
Development phase
247
Enrollment target

NCT03500198: Completed NA study, sponsored by Johnson & Johnson Surgical Vision.

NCT03500198 is a NA study that has completed, run by Johnson & Johnson Surgical Vision. The registered enrollment target is 247 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03500198, a NA study, has completed, sponsored by Johnson & Johnson Surgical Vision.

COMPLETED
Registry status
NA
Development phase
247 participants
Enrollment target

Study Summary

An investigational IOL designed to provide improved intermediate and near visual acuity and decreased spectacle wear was evaluated for safety and effectiveness in a six-month study.

Primary Outcome

Visual Acuity (VA) was assessed monocularly (each eye separately) under photopic (well-lit) conditions using best distance correction (distance refraction) and high contrast, Early Treatment Diabetic Retinopathy Study (ETDRS) chart at 66 cm from spectacle plane. It was measured in logarithm of the minimum angle of resolution (logMAR), on an ETDRS chart. A lower numeric value represented better VA. This analysis was pre-specified for the first operative eye only.

Interventions

  • DEVICE Investigational Intraocular Lens Device #1: Next Generation TECNIS IOL
  • DEVICE Control Monofocal Intraocular Lens: TECNIS Monofocal IOL

Trial Details

FieldValue
Enrollment Target 247 participants
Start Date 2018-06-28
Est. Completion 2019-06-05
Phase NA
Johnson & Johnson Surgical Vision

22 total trials

What the finished NCT03500198 record still lists

NCT03500198 is an interventional study that assigns participants to a tested intervention. The registered 247 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 2 interventions - of which Investigational Intraocular Lens Device #1: Next Generation TECNIS IOL is the first listed.

NCT03500198 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03500198 about?

NCT03500198 is a clinical study titled "Clinical Investigation of the Next Generation Intraocular Lens". An investigational IOL designed to provide improved intermediate and near visual acuity and decreased spectacle wear was evaluated for safety and effectiveness in a six-month study.

What is the current status of trial NCT03500198?

This trial is currently completed. It is a NA study. The enrollment target is 247 participants. The study started on 2018-06-28. Estimated completion is 2019-06-05.

What interventions are being tested in trial NCT03500198?

The interventions under investigation include: Investigational Intraocular Lens Device #1: Next Generation TECNIS IOL (DEVICE), Control Monofocal Intraocular Lens: TECNIS Monofocal IOL (DEVICE).

Who is sponsoring clinical trial NCT03500198?

This trial is sponsored by Johnson & Johnson Surgical Vision, which has 22 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03500198's enrollment target sits among peer trials

247 436th of 2000 higher than 1,565 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03500198, the US trial registry maintained by the National Library of Medicine. NCT03500198 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.