Clinical Study Protocol for the Assessment of Safety and Efficacy of the BARICLIP®

Advanced Bariatric Technology

Status

Not yet enrolling

Conditions

Overweight and Obesity

Treatments

Device: BariClip® Device Treatment

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT06338709

11-002

Details and patient eligibility

About

Overweight and obesity are at epidemic proportions in the world population as well as in the United States, where nearly 42% of the adult population(1) is considered to meet the definition of obesity, namely a body mass index ("BMI") ≥ 30 kg/m2. Well-established links between obesity and increased morbidities and mortality make treatment of the utmost importance; however, there continues to be a significant unmet need for more effective treatments for obesity. Bariatric surgery is recognized as an effective treatment for obese patients, particularly in more severe cases where surgical restriction of the stomach's capacity and outlet size are considered necessary. The BariClip® is a laparoscopically implanted device for treatment of obesity and serves as an alternative to current existing technology for use in bariatric surgery. The BariClip® is a medical device, non-adjustable, resembling a clip that is placed parallel to the greater curvature of the stomach, causing restriction of the gastric lumen in a vertical fashion. This multi-center, randomized, moderate-lifestyle (program of diet and exercise) controlled pivotal study of the BariClip® device is intended to gather data to objectively support its safety and effectiveness for the treatment of obesity in adults and to ultimately support marketing authorization of this device as a viable alternative to existing bariatric surgical procedures. Specifically, this study aims to look at efficacy of the BariClip® device with regards to weight loss metrics and secondary health metrics and safety of the BariClip® device with regards to serious adverse events.

Enrollment

165 estimated patients

Sex

All

Ages

22 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥22 years and ≤65 years
Have signed an Informed Consent Form
BMI 30-34.9 (with comorbidity) and 35-45 (with or without comorbidity) kg/m2
Willing to comply with study requirements
Subjects of childbearing potential not intending to become pregnant for the duration of their trial participation, with a documented negative pregnancy test and documentation of contraception confirmation and method
History of obesity and being overweight (BMI >30kg/m2) for at least 1 year
History of failure of non-surgical weight loss methods
Fully ambulatory without any severe chronic orthopedic disease that requires reliance on crutches, walkers or a wheelchair that could preclude exercise during the study

Exclusion criteria

Previous use of any device for the treatment of obesity
Known hepatic disease or biliary disease prior to screening (e.g., viral, autoimmune, fibrosis /cirrhosis etiology, but not including incidental fatty liver)
Known infection at time of randomization
Enrolled in another investigational obesity study
Uncorrectable bleeding diathesis, platelet dysfunction, thrombocytopenia with platelet counts less than 100,000/microliter, or known coagulopathy
Current substance abuse, alcohol or drug addiction
Chronic pancreatitis or acute pancreatitis within 12 months of randomization
Diagnosis of autoimmune connective tissue disorder (e.g., lupus erythematosus, scleroderma)
Type I diabetes
Hiatal hernia > 3cm
Presence of ulcer in stomach
Severe esophagitis (LA classification grade C or D)
Presence of Barrett's esophagus
Presence of any other abnormality that impacts the placement of the BariClip®
Taking Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) (e.g., aspirin, ibuprofen, etc.) within 10 days prior to randomization and/or there is a need or expected need to use during the first 12 months after the index procedure
Taking prescription antithrombotic therapy (e.g., anticoagulant, or antiplatelet agent) within 10 days prior to randomization and/or there is a need or expected need to use during the first 12 months after the index procedure
Taking any of the medications on the list of Excluded Medications within 30 days prior to randomization and/or there is a need or expected need to use these medications during the first 12 months after the enrollment