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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03392532
Other study ID # CLC127-C001
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 4, 2018
Est. completion date January 26, 2018

Study information

Verified date January 2019
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to compare the performance of two different types of Alcon soft toric study contact lenses to obtain information on study lens orientation.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date January 26, 2018
Est. primary completion date January 26, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Successful wear of soft contact lenses for vision correction in both eyes during the past 3 months for a minimum of 3 days per week and 8 hours per day

- Astigmatism

- Requires contact lenses

- Best corrected visual acuity of 20/25 or better in each eye

- Other protocol-specified inclusion criteria may apply

Exclusion Criteria:

- Any eye condition that contraindicates contact lens wear, as determined by the Investigator

- Any eye surgery that contraindicates contact lens wear, as determined by the Investigator

- Other protocol-specified exclusion criteria may apply

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Lotrafilcon B toric contact lenses with HYDRAGLYDE
Silicone hydrogel soft contact lenses for astigmatism
Lotrafilcon B toric contact lenses
Silicone hydrogel soft contact lenses for astigmatism

Locations

Country Name City State
United States Alcon Investigative Site Johns Creek Georgia

Sponsors (1)

Lead Sponsor Collaborator
Alcon Research

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Lenses With Axis Orientation Within ±30 Degrees From the 90 Degree Axis (Ideal Location) Each lens was classified based on whether the absolute difference between the axis location and 90° was less than or equal to 30° (ie, lens axis located between the 60° and 120° axis inclusive). Inferential testing was not planned for this primary effectiveness endpoint. Day 1, 10 minutes after lens insertion, each product
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