73
Participants
Start Date
January 5, 2015
Primary Completion Date
August 31, 2016
Study Completion Date
September 30, 2016
g-Cath EZ™ Suture Anchor Delivery Catheter
This is a multicenter, un-blinded, open label, pivotal supplemental study to G130163 intended to evaluate the safety and efficacy of treating previous sham subjects in the Essential pivotal trial (IDE#G130163) with the active treatment (the placement of g-Cath EZ suture anchors along with diet and exercise). Compliant sham subjects (those who attended all primary IDE follow-up visits AND who continue to meet eligibility criteria as described in this protocol) will be offered this active treatment after their 12 month unblinding visit in the Essential pivotal trial.
Lexington Medical Center, West Columbia
Hamilton Medical Center, Dalton
University of Miami Hospital, Miami
Baptist Memorial Hospital, Memphis
Fairview UMMC-University, Minneapolis
Northshore/Evanston Hospital, Evanston
WA University School of Medicine, St Louis
Saint Luke's Hospital, Kansas City
Crescent City Surgical, Metairie
Shea Campus -Scottsdale Healthcare, Scottsdale
Brigham & Women's Hospital, Boston
USGI Medical
INDUSTRY