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NCT07084545 · ClinicalTrials.gov registry record
Evaluation of Cataract Surgery Outcomes in Patients With Prior Laser Vision Correction Implanted With the CT LUCIA Lens
A clinical trial of Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction, sponsored by Carl Zeiss Meditec.
- Recruiting
- Registry status
- 30
- Enrollment target
- 2
- Study locations
NCT07084545 is a study of Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction that is actively recruiting participants, run by Carl Zeiss Meditec. The registered enrollment target is 30 participants. The trial reports 2 study locations across 2 states.
The verdict
NCT07084545, a study of Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction, is actively recruiting participants, sponsored by Carl Zeiss Meditec.
- RECRUITING
- Registry status
- 30 participants
- Enrollment target
- 2
- Study locations
Study Summary
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.
Conditions Studied
Interventions
- DEVICE CT LUCIA 621P Intraocular Lens Implantation
Study Locations (2)
Texas
- Berkeley Eye Center - Sugar Land
Virginia
- Piedmont Eye Center - Lynchburg
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2025-07 |
| Est. Completion | 2026-09 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07084545
The ClinicalTrials.gov registry entry for NCT07084545 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Carl Zeiss Meditec, which has 18 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction appearing as the primary indexed condition, and to 1 intervention - of which CT LUCIA 621P Intraocular Lens Implantation is the first listed.
NCT07084545 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Texas, Virginia.
Frequently Asked Questions
What is clinical trial NCT07084545 about?
NCT07084545 is a clinical study titled "Evaluation of Cataract Surgery Outcomes in Patients With Prior Laser Vision Correction Implanted With the CT LUCIA Lens". 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 e...
What is the current status of trial NCT07084545?
This trial is currently recruiting. The enrollment target is 30 participants. The study started on 2025-07. Estimated completion is 2026-09.
What conditions does trial NCT07084545 study?
This clinical trial studies the following conditions: Postoperative Visual Outcomes Following Cataract Surgery in Patients With Prior Myopic Corneal Laser Vision Correction.
What interventions are being tested in trial NCT07084545?
The interventions under investigation include: CT LUCIA 621P Intraocular Lens Implantation (DEVICE).
Who is sponsoring clinical trial NCT07084545?
This trial is sponsored by Carl Zeiss Meditec, which has 18 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07084545 being conducted?
This trial has 2 study locations across Texas, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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