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

NCT06967129 · ClinicalTrials.gov registry record · NA

Evaluation of Daily Disposable Toric Soft Lenses Manufactured With an Alternative Hydration Process

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

Completed
Registry status
NA
Development phase
281
Enrollment target

NCT06967129: Completed NA study, sponsored by Johnson & Johnson Vision Care.

NCT06967129 is a NA study that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 281 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06967129, a NA study, has completed, sponsored by Johnson & Johnson Vision Care.

COMPLETED
Registry status
NA
Development phase
281 participants
Enrollment target

Study Summary

This is a prospective, multi-site, dispensing, randomized, controlled, double-masked, bilateral wear, 2x2 crossover study to evaluate the safety and effectiveness of the test lens.

Primary Outcome

VA will be assessed monocularly under HLHC conditions at a test distance of 4 meters using ETDRS Charts.

Interventions

  • DEVICE Investigational daily disposable, soft, toric lenses manufactured on 4th Generation Technology (4GT) lines with extended mini-stack hydration using propylene glycol (PG) as the hydration solvent.
  • DEVICE ACUVUE® Oasys 1-Day for Astigmatism (AO1DfA) soft contact lenses manufactured on 3rd Generation Technology (3GT) legacy lines using isopropyl alcohol (IPA) as the hydration solvent.

Trial Details

FieldValue
Enrollment Target 281 participants
Start Date 2025-04-25
Est. Completion 2025-07-14
Phase NA
Johnson & Johnson Vision Care

142 total trials

What the finished NCT06967129 record still lists

NCT06967129 is an interventional study that assigns participants to a tested intervention. The registered 281 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 (80% lower).

The record links to 0 conditions, and to 2 interventions - of which Investigational daily disposable, soft, toric lenses manufactured on 4th Generation Technology (4GT) lines with extended mini-stack hydration using propylene glycol (PG) as the hydration solvent. is the first listed.

NCT06967129 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06967129 about?

NCT06967129 is a clinical study titled "Evaluation of Daily Disposable Toric Soft Lenses Manufactured With an Alternative Hydration Process". This is a prospective, multi-site, dispensing, randomized, controlled, double-masked, bilateral wear, 2x2 crossover study to evaluate the safety and effectiveness of the test lens.

What is the current status of trial NCT06967129?

This trial is currently completed. It is a NA study. The enrollment target is 281 participants. The study started on 2025-04-25. Estimated completion is 2025-07-14.

What interventions are being tested in trial NCT06967129?

The interventions under investigation include: Investigational daily disposable, soft, toric lenses manufactured on 4th Generation Technology (4GT) lines with extended mini-stack hydration using propylene glycol (PG) as the hydration solvent. (DEVICE), ACUVUE® Oasys 1-Day for Astigmatism (AO1DfA) soft contact lenses manufactured on 3rd Generation Technology (3GT) legacy lines using isopropyl alcohol (IPA) as the hydration solvent. (DEVICE).

Who is sponsoring clinical trial NCT06967129?

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 NCT06967129's enrollment target sits among peer trials

281 380th of 2000 higher than 1,621 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

  • NCT04521231 · 281 participants · Phase 1

    A Study of Subcutaneous Blinatumomab Administration in Participants With R/R and MRD+ B-ALL

  • NCT06190730 · 281 participants · NA

    REmote Symptom COllection to improVE postopeRative Care

  • NCT02860364 · 282 participants · NA

    Comparing Hypothermic Temperatures During Hemiarch Surgery

  • NCT04867395 · 282 participants · NA

    A Multi-Phase Study Examining Hospital to Home Transitions for Children With Medical Complexity

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 NCT06967129, the US trial registry maintained by the National Library of Medicine. NCT06967129 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.