Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04615507 · ClinicalTrials.gov registry record · NA
Evaluation of a Daily Disposable Novel Multifocal Contact Lens in a Myopic Population; Part 2
A NA study of Visual Acuity, sponsored by Johnson & Johnson Vision Care.
- Completed
- Registry status
- NA
- Development phase
- 71
- Enrollment target
- 6
- Study locations
NCT04615507: Completed NA study of Visual Acuity, sponsored by Johnson & Johnson Vision Care.
NCT04615507 is a NA study of Visual Acuity that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 71 participants, below the 137-participant average among 20 other Visual Acuity trials with a reported enrollment target (48% lower). The trial reports 6 study locations across 6 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04615507, a NA study of Visual Acuity, has completed, sponsored by Johnson & Johnson Vision Care.
- COMPLETED
- Registry status
- NA
- Development phase
- 71 participants
- Enrollment target
- 6
- Study locations
Study Summary
This is a 6-visit, subject-masked, multi-site, 2×3 crossover dispensing trial that will last approximately 2 - 4 months.
Primary Outcome
Binocular visual performance on logMAR (Logarithm of Minimal Angle of Resolution) scale was evaluated at distance (4 meters), intermediate (64 centimeters) and near (40 centimeters) under high luminance high contrast lighting condition using ETDRS (Early Treatment Diabetic Retinopathy Study) charts. The room illuminance was required to be between 7.3 and 7.9 EV (394-597 lux). For Distance (4 meters), the acceptable range for the chart luminance was 10.5-10.7 EV (181 208 cd/m2). For Intermediate
Conditions Studied
Interventions
- DEVICE JJVC Investigational Multifocal Contact Lens
- DEVICE Dailies Total 1® Multifocal Contact Lens
Study Locations (6)
Florida
- Vue Optical Boutique - Jacksonville
Georgia
- Visual Eyes, Inc. - Roswell
Missouri
- Advanced Eye Care - Raytown
New York
- Susquehanna Eye Care - Vestal
Ohio
- ProCare Vision Centers - Granville
Rhode Island
- West Bay Eye Associates - Warwick
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2020-10-09 |
| Est. Completion | 2020-12-09 |
| Phase | NA |
What the finished NCT04615507 record still lists
NCT04615507 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 137-participant average among 20 other Visual Acuity trials with a reported enrollment target (48% lower).
The record links to 1 condition, with Visual Acuity appearing as the primary indexed condition, and to 2 interventions - of which JJVC Investigational Multifocal Contact Lens is the first listed.
NCT04615507 lists 6 locations in 6 states (Florida, Georgia, Missouri).
Frequently Asked Questions
What is clinical trial NCT04615507 about?
NCT04615507 is a clinical study titled "Evaluation of a Daily Disposable Novel Multifocal Contact Lens in a Myopic Population; Part 2". This is a 6-visit, subject-masked, multi-site, 2×3 crossover dispensing trial that will last approximately 2 - 4 months.
What is the current status of trial NCT04615507?
This trial is currently completed. It is a NA study. The enrollment target is 71 participants. The study started on 2020-10-09. Estimated completion is 2020-12-09.
What conditions does trial NCT04615507 study?
This clinical trial studies the following conditions: Visual Acuity.
What interventions are being tested in trial NCT04615507?
The interventions under investigation include: JJVC Investigational Multifocal Contact Lens (DEVICE), Dailies Total 1® Multifocal Contact Lens (DEVICE).
Who is sponsoring clinical trial NCT04615507?
This trial is sponsored by Johnson & Johnson Vision Care, which has 142 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04615507 being conducted?
This trial has 6 study locations across Florida, Georgia, Missouri, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Visual Acuity
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT04615507's enrollment target sits among peer trials
71 15th of 20 higher than 5 of 20 other Visual Acuity trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Visual Acuity 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
-
Evaluation of Effect of Scatter on Visual Performance
RECRUITING · NA
-
Clinical Evaluation of a Reusable Multifocal Optical Design in a Presbyopic Population Phase 2
COMPLETED · NA
-
Evaluation of Daily Disposable Silicone Hydrogel Multifocal Toric Contact Lenses
COMPLETED · NA
-
Pilot Dispensing Study of Two Marketed Daily Disposable Multifocal Contact Lenses
COMPLETED · NA
-
Clinical Evaluation of Approved Contact Lenses
COMPLETED · NA
-
Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL
COMPLETED · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT05452889 · 71 participants · Early Phase 1
PET Image in PAH Patients
- NCT05766943 · 71 participants · NA
Reduction of Myopotential Interference With Smart Pass in S-ICD Patients
- NCT06229678 · 71 participants · Early Phase 1
Ketones, SGLT2, HFrEF
- NCT06377566 · 71 participants · Phase 2
A Study of BV-AVD in People With Bulky Hodgkin Lymphoma
Similar registry start date
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia
- NCT07125183 · started 2026-12 · Phase 2
Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma
- NCT07292298 · started 2026-11 · Phase 2
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
- NCT04263285 · started 2026-10 · NA
Treatment of Depression Post-SCI