f Post-Approval Studies (PAS) Database
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Post-Approval Studies (PAS) Database
  • Print
  • Share
  • E-mail
-

The FDA has the authority to require sponsors to perform a post-approval study (or studies) at the time of approval of a premarket approval (PMA), humanitarian device exemption (HDE), or product development protocol (PDP) application. Post-approval studies can provide patients, health care professionals, the device industry, the FDA and other stakeholders information on the continued safety and effectiveness (or continued probable benefit, in the case of an HDE) of approved medical devices. This database allows you to search Post-Approval Study information by applicant or device information.

Learn more...


           

Registry Study


Suggest Enhancement / Report Issue | export reports to excelExport to Excel
General
Study Status Redesigned/Replaced Study
Application Number /
Requirement Number		 P080030 / PAS003
Date Original Protocol Accepted 06/25/2012
Date Current Protocol Accepted 07/21/2015
Study Name Registry Study
Device Name GLAUKOS ISTENT TRABECULAR BYPASS STENT MODEL GTS100R/L
General Study Protocol Parameters
Study Design Active Surveillance
Data Source Sponsor Registry
Comparison Group No Control
Analysis Type Descriptive
Detailed Study Protocol Parameters
Study Objectives This study is a prospective, single쳌]arm, multicenter registry of subjects implanted with GTS100 stents. Subjects will be followed for at least 3 months and up to 12 months from the date of implantation. The study will determine the rate
of sight쳌]threatening adverse events for up to 6 months after
surgery. The specific question this study will address is: What are the 3쳌]and 6쳌] month sight쳌]threatening adverse event rates after implanting the study device in conjunction with cataract surgery and the corresponding 95% confidence interval?
Study Population Subjects with implantation of GTS100 in conjunction with cataract surgery.
Sample Size Not specified
Key Study Endpoints Sight쳌]threatening adverse events
Follow-up Visits and Length of Follow-up 3 months or until adverse events related to the study procedure are resolved or stable,


Registry Study Reporting Schedule

Reporting Schedule
Report
Date Due
FDA Receipt
Date
Applicant's Reporting Status
six month report 12/24/2012 12/26/2012 Overdue/Received
one year report 06/25/2013 06/25/2013 On Time
18 month report 12/24/2013 01/27/2014 Overdue/Received
two year report 06/25/2014 06/24/2014 On Time
three year report 06/25/2015 06/24/2015 On Time


Contact Us
Mandated Studies Program
Food and Drug Administration
10903 New Hampshire Ave.
Silver Spring, MD 20993-0002
Email: MandatedStudiesPrograms@fda.hhs.gov

Additional Resources

-
-