Obesity
Conditions
Keywords
Weight Loss, Trans-oral Endoscopic Procedure, Gastric Plication
Brief summary
The Articulating Circular Endoscopic (ACE) Stapler is an investigational system using endoscopic guidance to trans-orally place plications in the stomach in obese subjects to reduce volume and expansion of the fundus and greater curve to abate hunger as part of a supervised weight reduction program. The primary objective of this study is to perform an evaluation of the safety of the plication procedure. The secondary objective of this study is to evaluate the preliminary efficacy of the ACE Stapler for the treatment of obesity over a 24 month follow-up period.
Detailed description
This study was originally sponsored by BaroSense, Inc (protocol 11-03). 69 subjects were enrolled and treated as part of the study at 6 centers in 4 countries outside the United States. On April 30, 2013 BaroSense Inc went out of business and the study was terminated with all participating centers' Ethics Committees. At the point of study termination, all patients were in the middle of post procedure follow-up. Boston Scientific has since acquired the technology and study and will re-initiate follow-up to 24 months in order to collect data to support the original safety and efficacy endpoints of the protocol. Only the 69 subjects previously enrolled and treated in BaroSense's protocol 11-03 will be eligible for participation in the Boston Scientific continued follow-up study (The ACE Follow-up Study protocol 90891629). The Boston Scientific protocol will be approved by participating centers' Ethics Committees and patients who choose to participate in The ACE Follow-up Study will need to sign a new, Ethics Committee Approved, informed consent form.
Interventions
PROCEDUREACE Stapler
The ACE Stapler is used endoscopically, and incorporates a unique tissue capture mechanism to produce large, permanent serosa to serosa plications in a completely trans-oral approach.
Sponsors
Boston Scientific Corporation
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No
Inclusion criteria
1. Subject, male or female, is age 18 to 50 years of age. 2. Subject must be able to understand and be willing to sign an informed consent document. 3. Subject must be willing and able to participate in all aspects of the study and agree to comply with all study requirements for the duration of the study. This includes availability of reliable transportation and sufficient time to attend all follow-up visits. 4. Subject has a BMI of 40 - 45 or 30 to 39.9 plus one or more co-morbid diseases expected to improve with weight loss, including but not limited to hypertension, dyslipidemia, obstructive sleep apnea, or diabetes mellitus. 5. Subject must be fully ambulatory, without chronic reliance on walking aids such as crutches, walkers or a wheelchair. 6. Subject must be of sufficient and stable medical health, as evaluated by the Principal Investigator. 7. Subject must have a primary care physician that will manage the subject for any co-morbid conditions throughout the study. 8. Subject must have failed standard obesity therapy of diet, exercise, behavior modification, and pharmacologic agents either alone or in combination, as assessed by an interview with a member of the study team at baseline. 9. Subject agrees to refrain from any type of reconstructive surgery that may affect body weight such as mammoplasty or abdominal lipoplasty or liposuction, during the trial.
Exclusion criteria
1. Subject has history of/or signs and/or symptoms of gastro-duodenal ulcer disease. 2. Subject has poorly controlled diabetes as indicated by the lack of stable diabetes medications and doses over the last month, or has a history of diabetes for greater than 10 years. 3. Subject has had significant weight loss in the last 3 months, or between baseline and the study procedure. 4. Subject has a history or is diagnosed with eating disorders. 5. Subject has history of peptic ulcer and tests positive for H. pylori, unless treated before the procedure. 6. Subject has symptomatic congestive heart failure, cardiac arrhythmia or unstable coronary artery disease. 7. Subject has pre-existing respiratory disease such as chronic obstructive pulmonary disease (COPD), pneumonia or cancer. 8. Subject has significant esophageal disease including Zenker's diverticulum, grade 3-4 reflux esophagitis, stricture, Barrett's esophagus, esophageal cancer, esophageal diverticulum, dysphagia, achalasia, or symptoms of dysmotility. 9. Subject is observed during EGD to have heavily scarred, malignant or poor quality/friable tissue in areas of the stomach where plications are to be placed.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Safety | Enrollment through 24 months post-procedure. | The primary safety analysis will assess the occurrence and procedure relatedness of the following events: * Adverse Events (AE) * Adverse Device Effects (ADE) * Serious Adverse Events (SAE) * Unanticipated Adverse Device Effects (UADE) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Total weight lost (kg) and percent weight lost | Procedure through 24 months post-procedure | Relative to weight at the procedure visit. |
| Change in Body Mass Index (BMI) and percent change in BMI | Procedure through 24 months post-procedure | Relative to BMI at the procedure visit. |
| Change in waist circumference | Procedure through 24 months post-procedure | Relative to to waist circumference at the procedure visit. |
| Percent excess weight loss | Procedure through 24 months post-procedure | Percent excess weight loss (%EWL), defined as: (preoperative weight-current weight)/(preoperative weight - ideal weight) \*100, where ideal weight is the weight that would correspond to a BMI of 25 based on the subject's height. Relative to weight at the procedure visit. |
| Changes in Quality of Life | Enrollment through 24 months post-procedure | As reported on the SF-36 Quality of LIfe Questionnaire. |
| Changes in Feelings of Satiety | Enrollment through 24 months post-procedure | As reported on the TFEQ-R18 Three Factor Eating Questionnaire. |
| Improvement in co-morbid disease(s) | Enrollment through 24 months post-procedure | Including but not limited to, improvement in vital signs and/or laboratory values. |
Countries
Argentina, Canada, Israel, Netherlands
Outcome results
None listed