Venice, FLNCT07260695Now EnrollingIRB Ready

Cataract Clinical Trial in Venice, FL

Access cutting-edge cataract treatment through this phase 4 clinical trial at a research site in Venice. Study-provided care at no cost to qualified participants.

Sponsored by Center For Sight

Quick Self-Assessment

See if you qualify for this Venice location

Preparing your pre-screening questions…

Expert Care in Venice

Access cataract specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related cataract treatment provided free

Apply for This Venice Location

Check if you qualify for this cataract clinical trial in Venice, FL

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Venice

    Convenient for FL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Venice site if eligible
  4. 4Begin participation

About This Cataract Study in Venice

This prospective study evaluates the visual and refractive outcomes of the TECNIS Odyssey intraocular lens (IOL) implanted in patients with a history of myopic LASIK. Given the unique optical challenges of post-LASIK eyes, including altered corneal curvature and higher-order aberrations, the study aims to assess the IOL's performance in terms of distance, intermediate, and near vision, and patient satisfaction. Its design features may offer favorable outcomes in these patients.

Sponsor: Center For Sight

Who Can Participate

Inclusion Criteria

Subjects MUST fulfill the following conditions to qualify for enrollment into the trial
Age: 50 years and older.
Gender: Males and Females.
Bilateral cataracts
Bilateral implantation of Odyssey IOLs (toric and non-toric)
Scheduled to undergo standard cataract surgery in both eyes, within 1 to 30 days between surgeries.
Willing and able to provide written informed consent for participation in the study.
Willing and able to comply with scheduled visits and study examination procedures.
Postoperative best corrected visual acuity of 0.2 logMAR (20/32 Snellen) or better in each eye.

Exclusion Criteria

Subjects with ANY of the following conditions on the eligibility exam may NOT be enrolled into the trial.
Established ocular pathology, including: glaucoma (except glaucoma suspects), uveitis, and clinically-significant retinal pathology affecting the macula (with visual acuity worse than 20/25) and/or any other ocular findings that may, in the opinion of the investigator, affect vision.
Uncontrolled diabetes.
Use of any systemic or topical drug known to interfere with visual performance.
Any concurrent infectious/non-infectious conjunctivitis, keratitis or uveitis.
Clinically significant corneal dystrophy.
Contact lens use during the active treatment portion of the trial.
Irregular astigmatism.
Corneal irregularities potentially affecting visual acuity (i.e., keratoconus, corneal opacities
History of chronic intraocular inflammation.
History of retinal detachment.
Pseudoexfoliation syndrome or any other condition that has the potential to weaken the zonules.
Previous intraocular surgery.
Previous keratoplasty
Previous refractive surgery other than myopic LASIK or PRK (i.e., radial keratotomy, hyperopic LASIK, etc)
Severe dry eye.
Pupil abnormalities.
Subject who may reasonably be expected to require a secondary surgical intervention at any time during the study (other than YAG capsulotomy, i.e., LASIK).
Any clinically significant, serious, or severe medical or psychiatric condition that may interfere with the interpretation of study results.
Participation in (or current participation) any ophthalmic investigational drug or ophthalmic device trial within the previous 30 days prior to the start date of this trial.
Inability to focus or fixate for prolonged periods of time (e.g., due to strabismus, nystagmus, etc.)
Abnormal iris The principal investigator reserves the right to declare a patient ineligible or non-evaluable based on medical evidence that indicates the patient is unsuitable for the trial.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Venice?

Yes, this clinical trial (NCT07260695) has an active research site in Venice, FL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Cataract Treatment Options in Venice, FL

If you're searching for cataract treatment options in Venice, FL, this clinical trial (NCT07260695) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Venice research site is actively enrolling participants for this phase 4 clinical trial. You'll receive care from experienced cataract specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all cataract clinical trials near you to find additional studies recruiting in your area.

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