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COMPLETED NA

Comparing Effectiveness of the Hydrus Microstent (TM) to Two iStents to Lower IOP in Phakic Eyes

NCT02023242 · View on ClinicalTrials.gov ↗

Study Summary

This clinical trial compares two implantable devices intended to lower the pressure inside the eye of glaucoma patients.

Interventions

  • DEVICE Hydrus Microstent
  • DEVICE iStent Trabecular Micro Bypass

Study Locations (1)

California

  • Contact Richard Hope at Ivantis — Irvine

Trial Details

FieldValue
Enrollment Target 152 participants
Start Date 2012-10
Est. Completion 2018-01
Phase NA

Sponsor

Ivantis

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02023242

The ClinicalTrials.gov registry entry for NCT02023242 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 152 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ivantis, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Primary Open Angle Glaucoma appearing as the primary indexed condition, and to 2 interventions — of which Hydrus Microstent 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: NCT02023242 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 NCT02023242 about?

NCT02023242 is a clinical study titled "Comparing Effectiveness of the Hydrus Microstent (TM) to Two iStents to Lower IOP in Phakic Eyes". This clinical trial compares two implantable devices intended to lower the pressure inside the eye of glaucoma patients.

What is the current status of trial NCT02023242?

This trial is currently completed. It is a NA study. The enrollment target is 152 participants. The study started on 2012-10. Estimated completion is 2018-01.

What conditions does trial NCT02023242 study?

This clinical trial studies the following conditions: Primary Open Angle Glaucoma, Pigmentary Glaucoma, Pseudoexfoliative Glaucoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02023242?

The interventions under investigation include: Hydrus Microstent (DEVICE), iStent Trabecular Micro Bypass (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02023242?

This trial is sponsored by Ivantis, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02023242 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial