Lynchburg, VANCT07084545Now EnrollingIRB Ready

Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction Clinical Trial in Lynchburg, VA

Access cutting-edge postoperative visual outcomes following cataract surgery in patients with prior myopic corneal laser vision correction treatment through this clinical trial at a research site in Lynchburg. Study-provided care at no cost to qualified participants.

Sponsored by Carl Zeiss Meditec AG

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Expert Care in Lynchburg

Access postoperative visual outcomes following cataract surgery in patients with prior myopic corneal laser vision correction specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related postoperative visual outcomes following cataract surgery in patients with prior myopic corneal laser vision correction treatment provided free

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Check if you qualify for this postoperative visual outcomes following cataract surgery in patients with prior myopic corneal laser vision correction clinical trial in Lynchburg, VA

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Why Participate?

  • No-Cost Study Care

  • Local to Lynchburg

    Convenient for VA 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 Lynchburg site if eligible
  4. 4Begin participation

About This Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction Study in Lynchburg

This is a prospective, Phase IV, post-approval observational study evaluating postoperative outcomes in patients with a history of myopic corneal laser vision correction (LVC) undergoing bilateral cataract surgery with implantation of the CT LUCIA 621P intraocular lens (IOL). Up to 30 subjects (60 eyes) will be enrolled across up to three U.S. investigational sites. The study will assess visual and refractive outcomes, including biometry, manifest refraction, and patient-reported visual function over a 3-month follow-up period.

Sponsor: Carl Zeiss Meditec AG

Who Can Participate

Inclusion Criteria

Be at least 18 years of age or older.
Previous cornea LVC surgery performed at least 1 year before the implantation of the CT LUCIA 621P IOL, such as Laser-Assisted Intrastromal Keratomileusis (LASIK), Laser-Assisted Subepithelial Keratectomy (LASEK), Photorefractive Keratectomy (PRK) or Small Incision Lenticule Extraction (SMILE) for mild to moderate myopia, with or without astigmatism (up to, but not including, -6.0 D sphere in any meridian for myopic ablations.
Presenting for planned bilateral cataract extraction with in-the-bag posterior chamber IOL implantation, via phacoemulsification with or without femtosecond laser assisted cataract surgery (FLACS). Astigmatism management techniques, such as Astigmatic Keratotomy (AK), may be utilized during cataract surgery to target a predicted postoperative cylinder less than 0.75 D.
Clear intraocular media other than cataract (i.e., no hyphema, vitreous hemorrhage).
No visual acuity limiting corneal or retinal pathologies.
Able to and having provided written informed consent and a signed Health Insurance Portability and Accountability Act (HIPAA) form.
Availability, willingness, ability, and sufficient cognitive awareness to comply with study examination procedures and the schedule for study visits and evaluations.

Exclusion Criteria

Implantation of an IOL other than the CT LUCIA 621P in one or both eyes.
Eyes with preoperative anterior corneal astigmatism of ΔTK ≥1.00 D as measured by the IOLMaster 700 or with greater than 0.75 D predicted post-operative astigmatism at the spectacle plane.
Visual field loss which has an impact on visual acuity.
Subjects with diagnosed degenerative visual disorders (e.g., macular degeneration or other retinal disorders) that would confound visual acuity measurement.
Subjects with surgical complications in whom a CT LUCIA 621P IOL cannot be implanted in either eye.
Eyes with irregular corneal astigmatism, epithelial basement membrane dystrophy, chronic dry eye requiring continual treatment, underwent more than one LVC procedure in one or both eyes, or complications from the previous LVC which required additional surgical intervention.
Subjects with planned ocular surgery during the study (except Nd:YAG capsulotomy is permitted).
History of acute or chronic disease, pathology, illness, or ocular trauma that would, in the opinion of the investigator, confound results.
Current diagnosis of macular degeneration, cystoid macular edema, proliferative diabetic retinopathy, amblyopia, or other chronic ocular conditions that would confound the study results.
A current diagnosis of moderate or severe glaucoma.
Patients with strabismus, forme fruste keratoconus, keratoconus or other corneal pathologies that would confound visual acuity measurement.
Previous radial keratotomy (RK).
Previous corneal keratoplasty (e.g., corneal transplant, Descemet's stripping automated endothelial keratoplasty (DSAEK), lamellar keratoplasty).
Previous anterior or posterior chamber surgery (e.g., vitrectomy, laser iridotomy).
Pupil abnormalities (non-reactive, tonic pupils, abnormally shaped pupils, or pupils that do not dilate under mesopic/scotopic conditions).
Capsular or zonular abnormalities or other conditions that may affect the postoperative centration or tilt of the lens (e.g., pseudoexfoliation syndrome).
Usage of contact lenses during study participation.
Concurrent participation in another device investigation.

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 Lynchburg?

Yes, this clinical trial (NCT07084545) has an active research site in Lynchburg, VA 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.

Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction Treatment Options in Lynchburg, VA

If you're searching for postoperative visual outcomes following cataract surgery in patients with prior myopic corneal laser vision correction treatment options in Lynchburg, VA, this clinical trial (NCT07084545) 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 Lynchburg research site is actively enrolling participants for this clinical trial. You'll receive care from experienced postoperative visual outcomes following cataract surgery in patients with prior myopic corneal laser vision correction 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 postoperative visual outcomes following cataract surgery in patients with prior myopic corneal laser vision correction clinical trials near you to find additional studies recruiting in your area.

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