Contact Lens Trial Fitting Experience
ConditionPresbyopia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorCooperVision International Limited (CVIL)
About this trial
This study will assess a trial fitting experience with contact lenses.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
They are at least 40 years of age.
They understand their rights as a research participant and are willing and able to sign a Statement of Informed Consent.
They habitually wear MyDay sphere or MyDay Energys contact lenses (including sphere lenses for monovision, or sphere lenses for distance vision correction and spectacles for near vision correction).
They have a minimum reading add of +0.75DS (based on their manifest refraction) and no more than +2.50DS.
Disqualifiers
Is participating in any concurrent clinical or research trial.
They have an ocular disorder which would normally contraindicate contact lens wear.
They have a systemic disorder which would normally contraindicate contact lens wear.
They are pseudophakic or aphakic.
Trial design
Design model
Single group
Treatments tested in this trial
Lens A ( stenfilcon A )
Device15 minutes of daily wear
Treatment groups
25 Participants
are divided into 1 treatment groupGroup A: Lens A ( stenfilcon A)Experimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Participant Lens Fitting Experience
Participant's readiness to finalize a multifocal contact lens prescription after using an at home trial kit based on a scale of 1- 5 (1 - Good and 5 - Bad).
Time frame
At the End of 15 minutes of daily wearSponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: