Phase
Condition
Circulation Disorders
Vascular Diseases
Williams Syndrome
Treatment
N/AClinical Study ID
Ages 21-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
INCLUSION CRITERIA
Age 21-65
BMI ≥ 30 and ≤40 kg/m²
Willingness to comply with the substantial lifelong dietary restrictions required by the procedure
History of failure with non-surgical weight-loss methods
Willingness to follow protocol requirements, including signed informed consent, routine follow-up schedule, completing laboratory tests, and completing diet counseling
Residing within a reasonable distance from the investigator's office and able to travel to the investigator to complete all routine follow- up visits
Ability to give informed consent
Women of childbearing potential (i.e., not post-menopausal or surgically sterilized) must agree to use adequate birth control methods
***There will be a quota for at least a) 50 patients with hypertension on one or more anti-hypertensive medication, b) 50 patients with type II diabetes mellitus on oral agents only with HgA1c ≤ 9, and thus the cohort of 200 patients will be stratified into three groups (Obesity, Obesity HTH, Obesity DM) and block randomized. No more than 50 participants without comorbidities will be enrolled in the trial.
EXCLUSION CRITERIA
History of foregut or gastrointestinal (GI) surgery (except uncomplicated cholecystectomy or appendectomy)
Prior gastrointestinal surgery with sequelae, i.e. obstruction, and/or adhesive peritonitis or known abdominal adhesions.
Prior open or laparoscopic bariatric surgery.
Prior surgery of any kind on the esophagus, stomach or any type of hiatal hernia surgery.
Any inflammatory disease of the gastrointestinal tract including esophagitis, Barrett's esophagus, gastric ulceration, duodenal ulceration, cancer or specific inflammation such as Crohn's disease.
Potential upper gastrointestinal bleeding conditions such as esophageal or gastric varices, congenital or acquired intestinal telangiectasis, or other congenital anomalies of the gastrointestinal tract such as atresias or stenoses.
A gastric mass or gastric polyps > 1 cm in size.
A hiatal hernia > 4cm of axial displacement of the z-line above the diaphragm or severe or intractable gastro-esophageal reflux symptoms.
A structural abnormality in the esophagus or pharynx such as a stricture or diverticulum that could impede passage of the endoscope.
Achalasia or any other severe esophageal motility disorder
Severe coagulopathy.
Insulin-dependent diabetes (either Type 1 or Type 2) or a significant likelihood of requiring insulin treatment in the following 12 months or a HgbA1C >= 9.
Subjects with any serious health condition unrelated to their weight that would increase the risk of endoscopy
Chronic abdominal pain
Motility disorders of the GI tract such as gross esophageal motility disorders, gastroparesis or intractable constipation
Hepatic insufficiency or cirrhosis
Use of an intragastric device prior to this study due to the increased thickness of the stomach wall preventing effective suturing.
Active psychological issues preventing participation in a life-style modification program as determined by a psychologist
Patients unwilling to participate in an established medically-supervised diet and behavior modification program, with routine medical follow-up.
Patients receiving daily prescribed treatment with high dose aspirin (> 80mg daily), anti-inflammatory agents, anticoagulants or other gastric irritants.
Patients who are unable or unwilling to take prescribed proton pump inhibitor medication
Patients who are pregnant or breast-feeding.
Subjects with Severe cardiopulmonary disease or other serious organic disease which might include known history of coronary artery disease, Myocardial infarction within the past 6 months, poorly-controlled hypertension, required use of NSAIDs
Subjects taking medications on specified hourly intervals that may be affected by changes to gastric emptying, such as anti-seizure or anti-arrhythmic medications
Subjects who are taking corticosteroids, immunosuppressants, and narcotics
Subjects who are taking diet pills
Symptomatic congestive heart failure, cardiac arrhythmia or unstable coronary artery disease.
Pre-existing respiratory disease such as chronic obstructive pulmonary disease (COPD), pneumonia or cancer.
Diagnosis of autoimmune connective tissue disorder (e.g. lupus, erythematous, scleroderma) or immunocompromised.
Specific diagnosed genetic disorder such as Prader Willi syndrome.
Eating disorders including night eating syndrome (NES), bulimia, binge eating disorder, or compulsive overeating
Known history of endocrine disorders affecting weight such as uncontrolled hypothyroidism.
Study Design
Connect with a study center
Orlando Health
Orlando, Florida 32806
United StatesSite Not Available
University of Chicago
Chicago, Illinois 60637
United StatesSite Not Available
NorthShore University Health System
Evanston, Illinois 60201
United StatesSite Not Available
Johns Hopkins University
Baltimore, Maryland 21224
United StatesSite Not Available
Brigham and Women's Hospital
Boston, Massachusetts 02115
United StatesSite Not Available
Mayo Clinic in Rochester
Rochester, Minnesota 55905
United StatesSite Not Available
Cornell University
New York, New York 10065
United StatesSite Not Available
Avera McKennan Hospital & University Health Center
Sioux Falls, South Dakota 57105
United StatesSite Not Available
University of Texas
Houston, Texas 77401
United StatesSite Not Available

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