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

NCT04310566 · ClinicalTrials.gov registry record · NA

Evaluation of a Daily Disposable Novel Multifocal Contact Lens in a Myopic Population

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

Completed
Registry status
NA
Development phase
67
Enrollment target

NCT04310566: Completed NA study, sponsored by Johnson & Johnson Vision Care.

NCT04310566 is a NA study that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 67 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04310566, a NA study, has completed, sponsored by Johnson & Johnson Vision Care.

COMPLETED
Registry status
NA
Development phase
67 participants
Enrollment target

Study Summary

This is a single-masked, crossover, randomized-controlled, dispensing clinical trial. A total of approximately 70 myopic eligible subjects will be targeted to complete the study.

Primary Outcome

Subjective Overall Quality of Vision was assessed using the Contact Lens User Experience™ (CLUE) questionnaire. CLUE is a validated patient-reported outcomes (PRO) questionnaire to assess patient- xperience 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 indicat

Interventions

  • DEVICE Dailies Total 1® Multifocal Contact Lens
  • DEVICE JJVC Investigational Multifocal Contact Lens (senofilcon A c3)

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2020-02-21
Est. Completion 2020-03-28
Phase NA
Johnson & Johnson Vision Care

142 total trials

What the finished NCT04310566 record still lists

NCT04310566 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 67 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which Dailies Total 1® Multifocal Contact Lens is the first listed.

NCT04310566 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04310566 about?

NCT04310566 is a clinical study titled "Evaluation of a Daily Disposable Novel Multifocal Contact Lens in a Myopic Population". This is a single-masked, crossover, randomized-controlled, dispensing clinical trial. A total of approximately 70 myopic eligible subjects will be targeted to complete the study.

What is the current status of trial NCT04310566?

This trial is currently completed. It is a NA study. The enrollment target is 67 participants. The study started on 2020-02-21. Estimated completion is 2020-03-28.

What interventions are being tested in trial NCT04310566?

The interventions under investigation include: Dailies Total 1® Multifocal Contact Lens (DEVICE), JJVC Investigational Multifocal Contact Lens (senofilcon A c3) (DEVICE).

Who is sponsoring clinical trial NCT04310566?

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 NCT04310566's enrollment target sits among peer trials

67 1139th of 2000 higher than 862 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

  • NCT03213002 · 67 participants · Phase 1

    Oral Capecitabine and Temozolomide (CAPTEM) for Newly Diagnosed GBM

  • NCT04115163 · 67 participants · Phase 2

    Biologically Optimized Infusion Schedule of Gemcitabine and Nab-Paclitaxel for the Treatment of Metastatic Pancreatic Cancer

  • NCT04315324 · 67 participants · Phase 1

    Study to Test OBI-3424 in Patients With T-Cell Acute Lymphoblastic Leukemia (T-ALL) or T-Cell Lymphoblastic Lymphoma (T-LBL)

  • NCT04532424 · 67 participants · NA

    Transcranial Magnetic Stimulation for Restricted and Repetitive Behavior in ASD

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 NCT04310566, the US trial registry maintained by the National Library of Medicine. NCT04310566 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.