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Completed Not applicable Interventional Results available

A Study to Assess Long-Term Safety of the CyPass Micro-Stent in Patients Completing the COMPASS Trial

ClinicalTrials.gov ID: NCT02700984

Public ClinicalTrials.gov record NCT02700984. 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 Oct 19, 2026, 2:24 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Observational Multicenter Clinical Study to Assess the Long-Term Safety of the CyPass Micro-Stent in Patients With Primary Open Angle Glaucoma Who Have Completed Participation in the COMPASS Trial

Brief summary

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

The purpose of this study is to evaluate the long-term safety of the CyPass Micro-Stent in subjects who completed Study Protocol TMI-09-01, COMPASS Trial.

Study identification

NCT ID
NCT02700984
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Alcon Research
Industry
Enrollment
282 participants

Conditions and interventions

Interventions

Device · Procedure

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
Mar 30, 2016 (Actual)
Primary completion
Apr 18, 2018 (Actual)
Completion
Apr 18, 2018 (Actual)
Last update posted
Jan 24, 2024

2016 – 2018

United States locations

U.S. sites
22
U.S. states
15
U.S. cities
22
Facility City State ZIP Site status
Alcon Investigative Site Glendale Arizona 85306 —
Alcon Investigative Site Fayetteville Arkansas 72704 —
Alcon Investigative Site La Jolla California 92037 —
Alcon Investigative Site Orange California 92868 —
Alcon Investigative Site Fort Collins Colorado 80525 —
Alcon Investigative Site Parker Colorado 80134 —
Alcon Investigative Site Boynton Beach Florida 33426 —
Alcon Investigative Site Cape Coral Florida 33904 —
Alcon Investigative Site Sioux City Iowa 51104 —
Alcon Investigative Site Garden City Kansas 67846 —
Alcon Investigative Site Boston Massachusetts 02111 —
Alcon Investigative Site St Louis Missouri 63131 —
Alcon Investigative Site Vineland New Jersey 08361 —
Alcon Investigative Site Cincinnati Ohio 45242 —
Alcon Investigative Site Oklahoma City Oklahoma 73104 —
Alcon Investigative Site Kingston Pennsylvania 18704 —
Alcon Investigative Site West Mifflin Pennsylvania 15122 —
Alcon Investigative Site Maryville Tennessee 37803 —
Alcon Investigative Site Nashville Tennessee 37232 —
Alcon Investigative Site Dallas Texas 75231 —
Alcon Investigative Site Fort Worth Texas 76102 —
Alcon Investigative Site San Antonio Texas 78229 —

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 NCT02700984, 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 Jan 24, 2024 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02700984 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →