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

Completed · Not applicable

Conditions studied: Primary Open Angle Glaucoma (POAG)

In brief

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.

Key facts

Study ID

NCT02700984

Run by

Alcon Research

People needed

282

Starts

2016-03-30

Expected to finish

2018-04-18

Last updated by the study team

2024-01-24

Who can join

Age: 45 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Completed the COMPASS Trial
• Understands study requirements and is willing to follow study instructions and return for study visits

You may not qualify if…

• Systemic disease that would put subject health at risk and/or prevent completion of required study visits.
• Early termination from the COMPASS Trial.

Where it is running

• Alcon Investigative Site — Glendale, Arizona, United States
• Alcon Investigative Site — Fayetteville, Arkansas, United States
• Alcon Investigative Site — La Jolla, California, United States
• Alcon Investigative Site — Orange, California, United States
• Alcon Investigative Site — Fort Collins, Colorado, United States
• Alcon Investigative Site — Parker, Colorado, United States
• Alcon Investigative Site — Boynton Beach, Florida, United States
• Alcon Investigative Site — Cape Coral, Florida, United States
• Alcon Investigative Site — Sioux City, Iowa, United States
• Alcon Investigative Site — Garden City, Kansas, United States
• Alcon Investigative Site — Boston, Massachusetts, United States
• Alcon Investigative Site — St Louis, Missouri, United States
• Alcon Investigative Site — Vineland, New Jersey, United States
• Alcon Investigative Site — Cincinnati, Ohio, United States
• Alcon Investigative Site — Oklahoma City, Oklahoma, United States
• Alcon Investigative Site — Kingston, Pennsylvania, United States
• Alcon Investigative Site — West Mifflin, Pennsylvania, United States
• Alcon Investigative Site — Maryville, Tennessee, United States
• Alcon Investigative Site — Nashville, Tennessee, United States
• Alcon Investigative Site — Dallas, Texas, United States
• Alcon Investigative Site — Fort Worth, Texas, United States
• Alcon Investigative Site — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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