Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03679741 · ClinicalTrials.gov registry record · NA

Initial Evaluation of Investigational Lenses Manufactured on a New Production Line

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

Completed
Registry status
NA
Development phase
126
Enrollment target

NCT03679741: Completed NA study, sponsored by Johnson & Johnson Vision Care.

NCT03679741 is a NA study that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 126 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (91% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03679741, a NA study, has completed, sponsored by Johnson & Johnson Vision Care.

COMPLETED
Registry status
NA
Development phase
126 participants
Enrollment target

Study Summary

This study is a randomized, 4-visit, subject-masked, 2x3 bilateral crossover, dispensing trial. Each study lens will be worn bilaterally in a daily wear (DW) modality for at least 6 hours per day and 5 days per week for approximately two weeks each. The subject will wear either the Test or Control lens twice and the other study lens once.

Primary Outcome

Overall comfort was assessed using the Contact Lens User Experience™ (CLUE) questionnaire. CLUE is a validated patient-reported outcomes (PRO) questionnaire to assess patient-experience attributes of soft contact lenses (comfort, vision, handling, and packaging) in a contact-lens wearing population in the US, ages 18-65. Derived CLUE scores using Item Response Theory (IRT) follow a normal distribution with a population average score of 60 (SD 20), where higher scores indicate a more favorable/po

Interventions

  • DEVICE CONTROL Lens
  • DEVICE TEST Lens

Trial Details

FieldValue
Enrollment Target 126 participants
Start Date 2018-08-29
Est. Completion 2018-10-31
Phase NA
Johnson & Johnson Vision Care

142 total trials

What the finished NCT03679741 record still lists

NCT03679741 is an interventional study that assigns participants to a tested intervention. The registered 126 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 (91% lower).

The record links to 0 conditions, and to 2 interventions - of which CONTROL Lens is the first listed.

NCT03679741 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03679741 about?

NCT03679741 is a clinical study titled "Initial Evaluation of Investigational Lenses Manufactured on a New Production Line". This study is a randomized, 4-visit, subject-masked, 2x3 bilateral crossover, dispensing trial. Each study lens will be worn bilaterally in a daily wear (DW) modality for at least 6 hours per day and 5 days per week for approximately two weeks each. The subject will wear either the Test or Control l...

What is the current status of trial NCT03679741?

This trial is currently completed. It is a NA study. The enrollment target is 126 participants. The study started on 2018-08-29. Estimated completion is 2018-10-31.

What interventions are being tested in trial NCT03679741?

The interventions under investigation include: CONTROL Lens (DEVICE), TEST Lens (DEVICE).

Who is sponsoring clinical trial NCT03679741?

This trial is sponsored by Johnson & Johnson Vision Care, which has 142 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03679741's enrollment target sits among peer trials

126 749th of 2000 higher than 1,248 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

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

  • NCT01873131 · 126 participants · NA

    A Clinical Trial of Pulsed-dye Laser Versus Timolol Topical Solution Versus Observation on the Growth of Hemangioma in Newborn

  • NCT02621645 · 126 participants · Phase 4

    TRAP Intervention STudy: Early Versus Late Intervention for Twin Reversed Arterial Perfusion Sequence

  • NCT03838107 · 126 participants

    Markers of Trajectory in Pediatric CRPS

  • NCT03906422 · 126 participants · NA

    Comparison of Patient-reported Pain After Initial Archwire Placement

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

Source: ClinicalTrials.gov NCT03679741, the US trial registry maintained by the National Library of Medicine. NCT03679741 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.