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Corneal Collagen Cross-Linking for Ectasia (CXL)
NCT00674661 · View on ClinicalTrials.gov ↗
Study Summary
Prospective, randomized multicenter study to determine the safety and effectiveness of performing corneal collagen cross-linking (CXL) using riboflavin and UVA light in eyes with ectasia after refractive surgery.
Conditions Studied
Interventions
- DRUG riboflavin ophthalmic solution
- DEVICE UVA Irradiation
Study Locations (10)
California
- Shiley Eye Center — La Jolla
- Gordon -Weiss Vision Institute — San Diego
New York
- Edward Harkness Eye Institute at Columbia University Medical Center — New York
- Ophthalmic Consultants of Long Island — Rockville Centre
Florida
- Center for Excellence in Eye Care — Miami
Indiana
- Price Vision Group — Indianapolis
Kansas
- Durrie Vision — Kansas City
Maryland
- Wilmer Eye Institute at Johns Hopkins University — Baltimore
Minnesota
- Minnesota Eye Consultants — Minneapolis
New Jersey
- Cornea & Laser Eye Institute; Hersh Vision Group — Teaneck
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 130 participants |
| Start Date | 2007-12 |
| Est. Completion | 2011-11 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00674661
The ClinicalTrials.gov registry entry for NCT00674661 describes a study currently listed as completed. It is categorized as Phase 3, 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 130 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Glaukos Corporation, which has 45 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 Ectasia appearing as the primary indexed condition, and to 2 interventions — of which riboflavin ophthalmic solution 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: NCT00674661 reports 10 study locations spanning 8 distinct geographic areas — top geographies include California, New York, 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 NCT00674661 about?
NCT00674661 is a clinical study titled "Corneal Collagen Cross-Linking for Ectasia (CXL)". Prospective, randomized multicenter study to determine the safety and effectiveness of performing corneal collagen cross-linking (CXL) using riboflavin and UVA light in eyes with ectasia after refractive surgery.
What is the current status of trial NCT00674661?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 130 participants. The study started on 2007-12. Estimated completion is 2011-11.
What conditions does trial NCT00674661 study?
This clinical trial studies the following conditions: Ectasia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00674661?
The interventions under investigation include: riboflavin ophthalmic solution (DRUG), UVA Irradiation (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00674661?
This trial is sponsored by Glaukos Corporation, which has 45 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00674661 being conducted?
This trial has 10 study locations across California, Florida, Indiana, Kansas, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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