The purpose of this study is to evaluate the safety, technical feasibility, and initial effectiveness (i.e., weight loss primarily measured as percent excess weight loss) of TGVR performed using the Bard RESTORe Suturing System
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
18
Suturing in stomach
Brigham and Women's Hospital
Boston, Massachusetts, United States
Cleveland Clinic
Cleveland, Ohio, United States
Weight Loss
Time frame: 24 Months
Technical success of test procedure.
Time frame: 24 months
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