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CyPass Clinical Experience Study

NCT01097174 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 555

Last updated 2017-05-15

No results posted yet for this study

Summary

This study is to evaluate the long-term safety, effectiveness and clinical experience of the CyPass Micro-Stent in patients with glaucoma.

Conditions

  • Open Angle Glaucoma (OAG)

Interventions

DEVICE

CyPass Micro-Stent

The CyPass Micro-Stent is a small tube with a through-lumen designed to redirect aqueous fluid from the front into the back of they eye.

Sponsors & Collaborators

  • Transcend Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Tsontcho (Sean) Ianchulev, MD, MPH · Transcend Medical, Inc.

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2015-07-31
Completion
2015-07-31

Countries

  • Austria
  • Bulgaria
  • Germany
  • Italy
  • Poland
  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01097174 on ClinicalTrials.gov