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NCT07260695 · ClinicalTrials.gov registry record · Phase 4
Odyssey Evaluation in Post LASIK Patients
A Phase 4 study of Cataract, sponsored by Center For Sight.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT07260695 is a Phase 4 study of Cataract that is actively recruiting participants, run by Center For Sight. The registered enrollment target is 30 participants, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07260695, a Phase 4 study of Cataract, is actively recruiting participants, sponsored by Center For Sight.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Conditions Studied
Interventions
- DEVICE Odyssey intraocular lens
Study Locations (1)
Florida
- Center For Sight - Venice
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2025-08-18 |
| Est. Completion | 2026-08-18 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07260695
The ClinicalTrials.gov registry entry for NCT07260695 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (87% lower). The listed sponsor is Center For Sight, which has 5 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cataract appearing as the primary indexed condition, and to 1 intervention - of which Odyssey intraocular lens is the first listed.
NCT07260695 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT07260695 about?
NCT07260695 is a clinical study titled "Odyssey Evaluation in Post LASIK Patients". 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 a...
What is the current status of trial NCT07260695?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 30 participants. The study started on 2025-08-18. Estimated completion is 2026-08-18.
What conditions does trial NCT07260695 study?
This clinical trial studies the following conditions: Cataract.
What interventions are being tested in trial NCT07260695?
The interventions under investigation include: Odyssey intraocular lens (DEVICE).
Who is sponsoring clinical trial NCT07260695?
This trial is sponsored by Center For Sight, which has 5 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07260695 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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