Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01120782 · ClinicalTrials.gov registry record · NA
Non-dispensing Study to Check Prescription Equivalence of Two Daily Disposable Toric Contact Lens Types
A NA study of Astigmatism, sponsored by Johnson & Johnson Vision Care.
- Completed
- Registry status
- NA
- Development phase
- 45
- Enrollment target
- 2
- Study locations
NCT01120782 is a NA study of Astigmatism that has completed, run by Johnson & Johnson Vision Care. The registered enrollment target is 45 participants, below the 105-participant average among 31 other Astigmatism trials with a reported enrollment target (57% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT01120782, a NA study of Astigmatism, has completed, sponsored by Johnson & Johnson Vision Care.
- COMPLETED
- Registry status
- NA
- Development phase
- 45 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this study is to determine whether the prescription determined for a new daily disposable toric contact lens will be a good match to a prescription determined for an existing brand of lens.
Conditions Studied
Interventions
- DEVICE etafilcon A toric contact lens with new wetting agent
- DEVICE etafilcon A toric contact lens
Study Locations (2)
Florida
- - Jacksonville
New York
- - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2010-02-01 |
| Est. Completion | 2010-02-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01120782
The ClinicalTrials.gov registry entry for NCT01120782 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 105-participant average among 31 other Astigmatism trials with a reported enrollment target (57% lower). The listed sponsor is Johnson & Johnson Vision Care, which has 142 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Astigmatism appearing as the primary indexed condition, and to 2 interventions - of which etafilcon A toric contact lens with new wetting agent is the first listed.
NCT01120782 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, New York.
Frequently Asked Questions
What is clinical trial NCT01120782 about?
NCT01120782 is a clinical study titled "Non-dispensing Study to Check Prescription Equivalence of Two Daily Disposable Toric Contact Lens Types". The purpose of this study is to determine whether the prescription determined for a new daily disposable toric contact lens will be a good match to a prescription determined for an existing brand of lens.
What is the current status of trial NCT01120782?
This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2010-02-01. Estimated completion is 2010-02-01.
What conditions does trial NCT01120782 study?
This clinical trial studies the following conditions: Astigmatism.
What interventions are being tested in trial NCT01120782?
The interventions under investigation include: etafilcon A toric contact lens with new wetting agent (DEVICE), etafilcon A toric contact lens (DEVICE).
Who is sponsoring clinical trial NCT01120782?
This trial is sponsored by Johnson & Johnson Vision Care, which has 142 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01120782 being conducted?
This trial has 2 study locations across Florida, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Astigmatism
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.
-
Wavefront-guided LASIK Surgery Compared to Ray Tracing-Guided LASIK Surgery
RECRUITING · NA
-
A Three-Phase Contralateral Comparison of Ray-Tracing Guided LASIK Versus Three Other Refractive Surgery Platforms to Correct Myopia or Myopia With Astigmatism
RECRUITING · NA
-
Contoura With Phorcides Compared to Wavefront Optimized LASIK
RECRUITING · NA
-
Contralateral Study of Topography Guided LASIK Versus Small Incision Lenticule Extraction
ACTIVE NOT RECRUITING · NA
-
LASIK iDesign vs SMILE
ACTIVE NOT RECRUITING · NA
-
Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptix
ACTIVE NOT RECRUITING · NA
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.