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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 May 20, 2026, 3:53 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

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

  • Cataract Surgery Procedure
  • CyPass Micro-Stent Device

Procedure · Device

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 29, 2016
Primary completion
Apr 17, 2018
Completion
Apr 17, 2018
Last update posted
Jan 23, 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 23, 2024 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02700984 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →