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Evaluation of the Performance of Non-molded Soft Contact Lenses

U

University of Waterloo

Status and phase

Completed
Phase 3

Conditions

Ametropia

Treatments

Device: Soft contact lens

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00371787
P/240/06/CV

Details and patient eligibility

About

To evaluate the performance of the study soft lens for vision, comfort, physiology and lens surface properties.

Full description

To evaluate the performance of the study soft lens for vision, comfort, physiology and lens surface properties in a group of participants who present with lens related changes.

Enrollment

38 patients

Sex

All

Ages

17+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male or female, good health, age >17yrs, able to wear contact lenses as primary vision correction, able to see well and achieve good fit with study lens, has understood & signed consent form.

Exclusion criteria

  • Has active ocular disease, uses topical eye medication, wears gas permeable/silicone hydrogel /overnight wear contact lenses, is a participant in another clinical study, is deemed unsuitable for soft contact lens wear.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

38 participants in 2 patient groups

soft contact lens
Experimental group
Treatment:
Device: Soft contact lens
non-lens wear
No Intervention group
Description:
control group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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