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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02189863
Other study ID # M-14-009
Secondary ID
Status Completed
Phase N/A
First received July 11, 2014
Last updated January 21, 2016
Start date August 2014
Est. completion date December 2014

Study information

Verified date January 2016
Source Alcon Research
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

The overall objective of this study is to compare the effect on simulated driving performance of multifocal (MF) versus monovision (MV) soft contact lenses in mid-late presbyopes.


Description:

In this crossover study, subjects wore lotrafilcon B MV (AOAMV) and lotrafilcon B MF (AOAMF) soft contact lenses as randomized for 2 weeks each. Subjects were assessed using a standardised driving simulation for each of the two treatments. A fresh pair of lenses was dispensed for the assessment. Subjects also wore lotrafilcon B single vision distance (SVD) and comfilcon A MF contact lenses during Period 1 and Period 2 respectively for an additional same-day assessment. Habitual correction was worn for an acclimatization drive in the driving simulator during Period 1.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group N/A to 70 Years
Eligibility Inclusion Criteria:

- Current soft contact lens wearers (for 1 month or more) with distance spherical power requirements of +1.00 to + 4.00 diopters (D) or -1.00 to -10.00D, and who have never tried and then failed in monovision or AOAMF.

- Medium to high presbyopia, i.e. spectacle add requirement of +1.50D or more.

- Astigmatism, if present, =1.00D in both eyes.

- Distance visual acuity (VA) correctable to 20/30 (+0.2 logMAR) in both eyes.

- Within the normal ranges for binocular vision for distance (8? exophoria, =8? esophoria), vertical phoria = 1.5? hypo or hyper.

- Full United Kingdom driving license held for at least 3 years, with at least 2000 miles driven per year.

- Willing to wear study lenses at least 5 days per week.

- Other protocol-defined inclusion criteria may apply.

Exclusion Criteria:

- Existing AIR OPTIX® Multifocal CL user.

- Sphere requirement in the range +0.75 to -0.75D in both eyes.

- Previous refractive surgery.

- Ocular/systemic medical condition or medical treatment contra-indicating contact lens wear or driving simulation.

- Participation in a clinical study within the past 30 days.

- Other protocol-defined exclusion criteria may apply.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator)


Related Conditions & MeSH terms


Intervention

Device:
Lotrafilcon B MF
Multifocal contact lenses worn in both eyes
Lotrafilcon B MV
Spherical contact lenses worn with 1 eye corrected for distance and 1 eye corrected for near
Lotrafilcon B SVD
Spherical contact lenses worn with both eyes corrected for distance
Comfilcon A MF
Multifocal contact lenses worn in both eyes
Habitual contact lenses
Contact lenses worn in both eyes per subject's habitual prescription

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Alcon Research

Outcome

Type Measure Description Time frame Safety issue
Primary Driving Reaction Time to Hazards (as Measured by Time to Brake, in Seconds) Driving reaction time to hazards was assessed during simulated night time driving and measured as time to brake, in seconds. One eye (study eye) contributed to the analysis. This outcome measure was prespecified for AOAMV and AOAMF. Week 2, each period No
Secondary Standard Deviation of Lateral Positioning The standard deviation of lateral positioning (staying in the lane) was assessed during simulated night time driving and measured as the distance of deviation from the reference point, in meters. This outcome measure is prespecified for AOAMV and AOAMF. Week 2, each period No
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