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Prolongation of Contact Lens Comfortable Wear Duration by CLM2 Topical Gel
NCT03994406 · View on ClinicalTrials.gov ↗
Study Summary
This study compares contact lens comfortable wear duration, and signs and symptoms of contact lens discomfort, test versus control.
Conditions Studied
Interventions
- DRUG CLM2 topical gel
- DRUG Placebo topical gel
Study Locations (1)
California
- UC Berkeley Clinical Research Center — Berkeley
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2019-06-27 |
| Est. Completion | 2019-10-30 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03994406
The ClinicalTrials.gov registry entry for NCT03994406 describes a study currently listed as completed. It is categorized as Phase 2, 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 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Glia, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Contact Lens Discomfort appearing as the primary indexed condition, and to 2 interventions — of which CLM2 topical gel 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: NCT03994406 reports 1 study location spanning 1 distinct geographic area — top geographies include California. 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 NCT03994406 about?
NCT03994406 is a clinical study titled "Prolongation of Contact Lens Comfortable Wear Duration by CLM2 Topical Gel". This study compares contact lens comfortable wear duration, and signs and symptoms of contact lens discomfort, test versus control.
What is the current status of trial NCT03994406?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2019-06-27. Estimated completion is 2019-10-30.
What conditions does trial NCT03994406 study?
This clinical trial studies the following conditions: Contact Lens Discomfort, Contact Lens-induced Corneal Disorder, Contact Lens Acute Red Eye, Contact Lens-induced Corneal Fluorescein Staining. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03994406?
The interventions under investigation include: CLM2 topical gel (DRUG), Placebo topical gel (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03994406?
This trial is sponsored by Glia, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03994406 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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