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Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refractive Errors
NCT01675479 · View on ClinicalTrials.gov ↗
Study Summary
Demonstrate that wavefront-guided LASIK using measurements from the iDesign System is safe and effective for the treatment of Hyperopia.
Conditions Studied
Interventions
- DEVICE LASIK correction of hyperopic refractive errors
Study Locations (9)
Missouri
- Pepose Vision Institute — Chesterfield
- Durrie Vision — Kansas City
California
- Maloney Vision Institute — Los Angeles
Florida
- University of Miami Bascom Palmer Eye Institute — Miami
Illinois
- Kraff Eye Institute — Chicago
New Mexico
- Coleman Vision — Albuquerque
Texas
- Lehmann Eye Center — Nacogdoches
Virginia
- The Eye Center — Fairfax
Washington
- King LASIK — Renton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 167 participants |
| Start Date | 2012-12-31 |
| Est. Completion | 2016-10-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01675479
The ClinicalTrials.gov registry entry for NCT01675479 describes a study currently listed as completed. 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 167 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Abbott Medical Optics, which has 3 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 Hyperopia appearing as the primary indexed condition, and to 1 intervention — of which LASIK correction of hyperopic refractive errors 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: NCT01675479 reports 9 study locations spanning 8 distinct geographic areas — top geographies include Missouri, California, Florida. 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 NCT01675479 about?
NCT01675479 is a clinical study titled "Safety and Effectiveness of Wavefront-Guided LASIK Correction of Hyperopic Refractive Errors". Demonstrate that wavefront-guided LASIK using measurements from the iDesign System is safe and effective for the treatment of Hyperopia.
What is the current status of trial NCT01675479?
This trial is currently completed. It is a NA study. The enrollment target is 167 participants. The study started on 2012-12-31. Estimated completion is 2016-10-31.
What conditions does trial NCT01675479 study?
This clinical trial studies the following conditions: Hyperopia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01675479?
The interventions under investigation include: LASIK correction of hyperopic refractive errors (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01675479?
This trial is sponsored by Abbott Medical Optics, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01675479 being conducted?
This trial has 9 study locations across California, Florida, Illinois, Missouri, New Mexico. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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