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Comprehensive Assessment of Multiple Products (CAMP)
NCT07276347 · View on ClinicalTrials.gov ↗
Study Summary
The aim of this study is to assess contact lens performance and acceptance.
Interventions
- DEVICE somofilcon A lens
- DEVICE stenfilcon A lens
- DEVICE fanfilcon A lens
- DEVICE comfilcon A lens
- DEVICE verofilcon A lens
Study Locations (1)
Indiana
- Indiana University — Bloomington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 250 participants |
| Start Date | 2025-12 |
| Est. Completion | 2026-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07276347
The ClinicalTrials.gov registry entry for NCT07276347 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 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is CooperVision International Limited (CVIL), which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Myopia appearing as the primary indexed condition, and to 5 interventions — of which somofilcon A lens 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: NCT07276347 reports 1 study location spanning 1 distinct geographic area — top geographies include Indiana. 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 NCT07276347 about?
NCT07276347 is a clinical study titled "Comprehensive Assessment of Multiple Products (CAMP)". The aim of this study is to assess contact lens performance and acceptance.
What is the current status of trial NCT07276347?
This trial is currently recruiting. It is a NA study. The enrollment target is 250 participants. The study started on 2025-12. Estimated completion is 2026-09.
What conditions does trial NCT07276347 study?
This clinical trial studies the following conditions: Myopia, 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 NCT07276347?
The interventions under investigation include: somofilcon A lens (DEVICE), stenfilcon A lens (DEVICE), fanfilcon A lens (DEVICE), comfilcon A lens (DEVICE), verofilcon A lens (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07276347?
This trial is sponsored by CooperVision International Limited (CVIL), which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07276347 being conducted?
This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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