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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: Recruiting Phase 4 study of Cataract, sponsored by Center For Sight.

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

The defocus curve assesses a patient's visual performance at various distances by introducing different levels of lens defocus (measured in diopters) and recording the corresponding visual acuity. It provides a comprehensive evaluation of the range of clear vision (distance, intermediate, and near) offered by an intraocular lens.

Conditions Studied

Interventions

  • DEVICE Odyssey intraocular lens

Study Locations (1)

Florida

  • Center For Sight - Venice

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-08-18
Est. Completion 2026-08-18
Phase Phase 4
Center For Sight

5 total trials

What NCT07260695 shows while recruiting

NCT07260695 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 228-participant average among 83 other Cataract trials with a reported enrollment target (87% lower).

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 a single indexed study location in 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.

Similar trials for Cataract

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07260695's enrollment target sits among peer trials

30 73rd of 83 higher than 9 of 83 other Cataract trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Cataract trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07260695, the US trial registry maintained by the National Library of Medicine. NCT07260695 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.