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

NCT03095027 · ClinicalTrials.gov registry record · NA

Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear

A NA study, sponsored by Alcon Research.

Completed
Registry status
NA
Development phase
54
Enrollment target

NCT03095027: Completed NA study, sponsored by Alcon Research.

NCT03095027 is a NA study that has completed, run by Alcon Research. The registered enrollment target is 54 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03095027, a NA study, has completed, sponsored by Alcon Research.

COMPLETED
Registry status
NA
Development phase
54 participants
Enrollment target

Study Summary

The purpose of this study is to compare the visual acuity of an investigational silicone hydrogel to a commercially available silicone hydrogel in contact lens wearers.

Primary Outcome

VA was assessed and collected using a Snellen chart. Conversion to logMAR (logarithm of the minimum angle of resolution) was performed. A logMAR acuity of 0.0 corresponds to 20/20 Snellen acuity, with a negative value denoting better than 20/20 visual acuity. Both eyes contributed to the analysis.

Interventions

  • DEVICE FID122819 contact lenses
  • DEVICE Stenfilcon A contact lenses

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2017-04-19
Est. Completion 2017-05-15
Phase NA
Alcon Research

275 total trials

What the finished NCT03095027 record still lists

NCT03095027 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 54 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which FID122819 contact lenses is the first listed.

NCT03095027 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03095027 about?

NCT03095027 is a clinical study titled "Clinical Performance of a Silicone Hydrogel for Daily Disposable Wear". The purpose of this study is to compare the visual acuity of an investigational silicone hydrogel to a commercially available silicone hydrogel in contact lens wearers.

What is the current status of trial NCT03095027?

This trial is currently completed. It is a NA study. The enrollment target is 54 participants. The study started on 2017-04-19. Estimated completion is 2017-05-15.

What interventions are being tested in trial NCT03095027?

The interventions under investigation include: FID122819 contact lenses (DEVICE), Stenfilcon A contact lenses (DEVICE).

Who is sponsoring clinical trial NCT03095027?

This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03095027's enrollment target sits among peer trials

54 1268th of 2000 higher than 730 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

  • NCT01269853 · 54 participants · Phase 1

    Repeated Super-selective Intraarterial Cerebral Infusion of Bevacizumab (Avastin) for Treatment of Relapsed GBM and AA

  • NCT02390752 · 54 participants · Phase 1

    Phase I Trial of TURALIO(R) (Pexidartinib, PLX3397) in Children and Young Adults With Refractory Leukemias and Refractory Solid Tumors Including Neurofibromatosis Type 1 (NF1) Associated Plexiform Neurofibromas (PN) and Tenosynovial Giant Cell Tumor ...

  • NCT02991248 · 54 participants · NA

    Improve Dynamic Lateral Balance of Humans With SCI

  • NCT02993900 · 54 participants · NA

    Image-Guided Gynecologic Brachytherapy

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 NCT03095027, the US trial registry maintained by the National Library of Medicine. NCT03095027 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.