MedDataX Logo

Evaluation of Two Daily Disposable Contact Lenses for Wearers With Astigmatism

NCT ID: NCT01207466

Last Updated: 2012-07-10

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

95 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-09-30

Study Completion Date

2010-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this trial is to compare the performance of two contact lenses for contact lens wearers with astigmatism.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Astigmatism Myopia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Nelfilcon A invest'l / nelfilconA comm'l

Nelfilcon A investigational toric contact lenses worn first, with nelfilcon A commercial toric contact lenses worn second. Each product worn bilaterally on a daily disposable basis for one week.

Group Type OTHER

Nelfilcon A investigational contact lens

Intervention Type DEVICE

Investigational, soft contact lens for astigmatism worn on a daily disposable basis.

Nelfilcon A commercial contact lens

Intervention Type DEVICE

Commercially marketed, soft contact lens for astigmatism worn on a daily disposable basis.

Nelfilcon A comm'l / nelfilconA invest'l

Nelfilcon A commercial toric contact lenses worn first, with nelfilcon A investigational toric contact lenses worn second. Each product worn bilaterally on a daily disposable basis for one week.

Group Type OTHER

Nelfilcon A investigational contact lens

Intervention Type DEVICE

Investigational, soft contact lens for astigmatism worn on a daily disposable basis.

Nelfilcon A commercial contact lens

Intervention Type DEVICE

Commercially marketed, soft contact lens for astigmatism worn on a daily disposable basis.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Nelfilcon A investigational contact lens

Investigational, soft contact lens for astigmatism worn on a daily disposable basis.

Intervention Type DEVICE

Nelfilcon A commercial contact lens

Commercially marketed, soft contact lens for astigmatism worn on a daily disposable basis.

Intervention Type DEVICE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Focus DAILIES Toric

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Currently wearing soft contact lenses with astigmatism correction

Exclusion Criteria

* Eye injury or surgery within twelve weeks prior to enrollment
* Currently enrolled in an ophthalmic clinical trial
* Strabismus
* Any use of medications for which contact lens wear could be contraindicated as determined by the investigator
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

CIBA VISION

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

P-415-C-001 sub 2

Identifier Type: -

Identifier Source: org_study_id