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Safety and Efficacy of Corneal Cross-linking in Subjects With Keratoconus
NCT05314738 · View on ClinicalTrials.gov ↗
Study Summary
Clinical Trial to Evaluate the Safety and Efficacy of Corneal Cross-linking in Subjects with Keratoconus.
Conditions Studied
Interventions
- COMBINATION_PRODUCT NXL Energy 1
- COMBINATION_PRODUCT NXL Energy 2
- COMBINATION_PRODUCT NXL Energy 3
- COMBINATION_PRODUCT Sham Treatment
Study Locations (3)
Alabama
- Glaukos Investigative Site — Dothan
New Jersey
- Glaukos Investigative Site — Teaneck
Ohio
- Glaukos Investigative Site — Westerville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2022-03-08 |
| Est. Completion | 2026-02 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05314738
The ClinicalTrials.gov registry entry for NCT05314738 describes a study currently listed as recruiting. It is categorized as Phase 1, 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 150 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 Progressive Keratoconus appearing as the primary indexed condition, and to 4 interventions — of which NXL Energy 1 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: NCT05314738 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Alabama, New Jersey, Ohio. 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 NCT05314738 about?
NCT05314738 is a clinical study titled "Safety and Efficacy of Corneal Cross-linking in Subjects With Keratoconus". Clinical Trial to Evaluate the Safety and Efficacy of Corneal Cross-linking in Subjects with Keratoconus.
What is the current status of trial NCT05314738?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 150 participants. The study started on 2022-03-08. Estimated completion is 2026-02.
What conditions does trial NCT05314738 study?
This clinical trial studies the following conditions: Progressive Keratoconus. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05314738?
The interventions under investigation include: NXL Energy 1 (COMBINATION_PRODUCT), NXL Energy 2 (COMBINATION_PRODUCT), NXL Energy 3 (COMBINATION_PRODUCT), Sham Treatment (COMBINATION_PRODUCT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05314738?
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 NCT05314738 being conducted?
This trial has 3 study locations across Alabama, New Jersey, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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