Visual Outcomes of Tecnis Symfony Opti-Blue EDOF Intraocular Lens (IOL) for Cataracts

This study is looking at how well a special lens, called the Tecnis Symfony Opti-Blue EDOF IOL, works for people having cataract surgery. This lens is designed to improve your vision at different distances (far, intermediate, and near) and reduce issues like glare and halos, especially at night. It does this by filtering out violet light. You might be able to join if you are between 50 and 85 years old, have cataracts, and also have certain retinal conditions, as long as your potential vision is good (20/30 or better). The study will measure your vision at these different distances three months after surgery to see how effective the lens is. The current status of this study is unclear.

Study design
This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 15 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Your visual acuity will be measured at distance, intermediate, and near three months after the surgery.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06500416

Visual Outcomes of Tecnis Symfony Opti-Blue EDOF Intraocular Lens (IOL)

Not Yet Recruiting
NAAges 50–85InterventionalTreatment
Coastal Eye Surgeons PLLC
~15 participants
Updated 2024-08-09 on ClinicalTrials.gov
What's tested:Tecnis Symfony OptiBlue/ Tecnis Symfony OptiBlue toric IOL

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Binocular uncorrected visual acuity at distance
Measured over 3 months
+2 more outcomes measured
Cataract
1 sites across 1 states
Connecticut1

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Patients diagnosed with retinal comorbidities, with visual acuity potential of 20/30 or better, who wish to undergo bilateral cataract surgery and are willing to provide written informed consent and adhere to study requirements.

Exclusion

Corneal dystrophies
Central corneal scarring
Keratoconus
Proliferative diabetic retinopathy
Exudative macular degeneration
Zonular weakness
Pseudoexfoliation
Fovea-involving atrophy
Severe dry eye
Amblyopia
Pupil abnormalities
Need for an IOL outside the range of +5.0 D to +34.0 D or cylinder power over 3.75 D
Patients who have undergone prior cataract surgery and IOL implantation in either eye; had prior corneal refractive or corneal transplantation surgery; diabetics post-vitrectomy; or who have a history of macula-off retinal detachment will also be excluded.
  • Binocular uncorrected visual acuity at distance3 months

    Mean binocular uncorrected visual acuity at distance

  • Binocular uncorrected visual acuity at intermediate3 months

    Mean binocular uncorrected visual acuity at intermediate

  • Binocular uncorrected visual acuity at near3 months

    Mean binocular uncorrected visual acuity at near