Obesity Clinical Trial
Official title:
A Prospective, Multicenter, Open-label, Post-approval Study of the Safety and Effectiveness of ORBERA365 as a 12-month Adjunct to Weight Reduction for Obese Adults or Pre-surgical Weight Reduction for Obese or Super-obese Adults
A prospective, multicenter, open-label, post-approval study of the safety and effectiveness of ORBERA36 as a 12-month adjunct to weight reduction for obese adults (BMI ≥ 27 kg/m2 and BMI ≤ 50 kg/m2) or for pre-surgical weight reduction in obese and super-obese adults (BMI ≥ 40 kg/m2 or ≥ 35 kg/m2 with comorbidities).
This is a prospective, multicenter, open label study of the safety and effectiveness of
ORBERA365™ for use as an adjunct to behavioral modification for obese adults (BMI ≥ 27 kg/m2
and BMI ≤ 50 kg/m2) or for pre-surgical weight reduction in obese and super-obese adults (BMI
≥ 40 kg/m2 or ≥ 35 kg/m2 with comorbidities). All study subjects will participate in a
behavioral modification program for 52 weeks, which will include a low calorie diet as well
as nutritional and behavior modification counseling. Subjects will have ORBERA365™ placed for
up to 52 weeks.
Evaluations while on treatment will be performed at baseline (pre-placement), Day 0
(ORBERA365 placement) and during monthly clinic visits during the 1st 6 months of device
therapy and at months 9 and ORBERA365 removal. All subjects will have a final study visit at
12 months, or study exit, whichever comes first. Device removal will occur at 52 unless
removed early by subject request and/or physician recommendation. Reasons for early removal
may include, but are not limited to, adverse events, subject dissatisfaction or achievement
of weight loss goal.
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