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Measuring Outcomes of LASIK and EVO-ICL in Matched Populations
NCT06700460 · View on ClinicalTrials.gov ↗
Study Summary
Evaluating outcomes after bilateral implantation of ICLs or bilateral LASIK as treatment options for the correction or reduction of myopia with or without astigmatism.
Conditions Studied
Interventions
- DEVICE Laser-assisted in Situ Keratomileusis
- DEVICE Implantable Collamer Lens placement
Study Locations (5)
Nebraska
- Kugler Vision — Omaha
Ohio
- Cleveland Eye Clinic — Cleveland
South Carolina
- Carolina Eyecare Physicians — Mt. Pleasant
South Dakota
- Vance Thompson Vision Clinic — Sioux Falls
Texas
- Slade & Baker Vision — Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 56 participants |
| Start Date | 2024-11-27 |
| Est. Completion | 2025-04-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06700460
The ClinicalTrials.gov registry entry for NCT06700460 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 56 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vance Thompson Vision, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 2 interventions — of which Laser-assisted in Situ Keratomileusis is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06700460 reports 5 study locations spanning 5 distinct geographic areas — top geographies include Nebraska, Ohio, South Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06700460 about?
NCT06700460 is a clinical study titled "Measuring Outcomes of LASIK and EVO-ICL in Matched Populations". Evaluating outcomes after bilateral implantation of ICLs or bilateral LASIK as treatment options for the correction or reduction of myopia with or without astigmatism.
What is the current status of trial NCT06700460?
This trial is currently recruiting. It is a NA study. The enrollment target is 56 participants. The study started on 2024-11-27. Estimated completion is 2025-04-01.
What conditions does trial NCT06700460 study?
This clinical trial studies the following conditions: Myopia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06700460?
The interventions under investigation include: Laser-assisted in Situ Keratomileusis (DEVICE), Implantable Collamer Lens placement (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06700460?
This trial is sponsored by Vance Thompson Vision, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06700460 being conducted?
This trial has 5 study locations across Nebraska, Ohio, South Carolina, South Dakota, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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