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Terminated Not applicable Interventional Results available

Post Approval Study of the CyPass System

ClinicalTrials.gov ID: NCT03273907

Public ClinicalTrials.gov record NCT03273907. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 8:17 PM EST

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Official title

Post Approval Study of the CyPass System in Patients With Primary Open Angle Glaucoma Undergoing Cataract Surgery

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to demonstrate that the rate of clinically relevant complications associated with CyPass Micro-Stent placement and stability using the CyPass 241-S applier, as determined at 36 months in the postmarket setting, is less than the pre-specified performance target, which is based on experience with the CyPass Model E applier in COMPASS trial TMI-09-01 (NCT01085357).

Study identification

NCT ID
NCT03273907
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Alcon Research
Industry
Enrollment
79 participants

Conditions and interventions

Eligibility (public fields only)

Age range
45 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 12, 2017 (Actual)
Primary completion
Aug 31, 2021 (Actual)
Completion
Aug 31, 2021 (Actual)
Last update posted
Feb 16, 2024

2017 – 2021

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Alcon Investigative Site Phoenix Arizona 85016 —
Alcon Investigative Site Orange California 92868 —
Alcon Investigative Site Fort Collins Colorado 80528 —
Alcon Investigative Site Jacksonville Florida 32256 —
Alcon Investigative Site Panama City Florida 32405 —
Alcon Investigative Site Gainesville Georgia 30501 —
Alcon Investigative Site Marietta Georgia 30060 —
Alcon Investigative Site Garden City Kansas 67846 —
Alcon Investigative Site Fraser Michigan 48026 —
Alcon Investigative Site St Louis Missouri 63131 —
Alcon Investivative Site St Louis Missouri 63141 —
Alcon Investigative Site Vineland New Jersey 08361 —
Alcon Investigative Site Bala-Cynwyd Pennsylvania 19004 —
Alcon Investigative Site Chambersburg Pennsylvania 17201 —
Alcon Investigative Site Austin Texas 78731 —
Alcon Investigative Site El Paso Texas 79902 —
Alcon Investigative Site Houston Texas 77030 —
Alcon Investigative Site Bellevue Washington 98004-3012 —
Alcon Investigative Site Kenosha Wisconsin 53142 —
Alcon Investigative Site Racine Wisconsin 53405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03273907, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 16, 2024 · Synced Nov 4, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03273907 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →