The USGI Medical ESSENTIAL Study for Weight Loss
Study Details
Study Description
Brief Summary
This is a multicenter, randomized, evaluator and subject blinded, parallel-group, controlled study intended to evaluate the safety and efficacy of treating obese patients with the placement of g-Cath EZ suture anchors followed by a structured diet and exercise plan as compared to a sham procedure followed by the same diet and exercise plan. Subjects will be randomly assigned in a 2:1 ratio to the treatment procedure followed by diet and exercise or the sham procedure followed by diet and exercise. After un-blinding at 12 months post-treatment, sham patients can choose to have the treatment procedure as well.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Treatment group The treatment of obese patients with the placement of g-Cath EZ suture anchors along with Diet and Exercise |
Device: placement of g-Cath EZ suture anchors
Other Names:
Behavioral: Diet and Exercise
A structured diet and exercise plan
|
| Sham Comparator: Sham Group The treatment of obese patients with the sham procedure along with Diet and Exercise |
Procedure: Sham procedure
Behavioral: Diet and Exercise
A structured diet and exercise plan
|
Outcome Measures
Primary Outcome Measures
- Total Body Weight Loss [Enrollment to 12 months]
Evaluate the effectiveness of the g-Cath EZ™ Suture Anchor Delivery Catheter (USGI Medical, San Clemente, CA, USA) with diet and exercise as an early weight loss intervention for Class I obesity subjects with at least one non-severe obesity related co-morbid condition or Class II obesity subjects with or without a non-severe obesity related co-morbid condition compared to a sham procedure, diet and exercise group.
Secondary Outcome Measures
- Quality of Life scores (IWQOL) [enrollment to 12 months]
Assessment of changes
- Comorbid status [Enrollment to 12 months]
Assessment of changes from baseline at 12 months in hypertension, diabetes, and hyperlipidemia
- Eating Behavior changes [Enrollment to 12 months]
assessment of changes from baseline at 12 months in eating behavior scores (TFEQ) and subjective changes in food capacity, hunger, and satiety in both study groups
Eligibility Criteria
Criteria
Inclusion Criteria:
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Provide written informed consent.
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Be male or female subjects between the ages of 22-60 years.
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If female, be either post-menopausal, surgically sterile or agree to practice birth control during year of study and have negative serum HCG at screening and baseline.
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Have a Body Mass Index (BMI) of ≥30 and <35 with at least one non-severe co-morbid obesity related condition or a BMI ≥ 35 and < 40 with or without a non-severe obesity related co-morbid condition, where a severe co-morbid condition is defined as severe if symptoms cause severe discomfort, performance of daily activities is compromised, and/or condition is not entirely controlled with prescription drug therapy.
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Have had no significant weight change (+/- 5% of total body weight) in last 6 months.
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Have an American Society Anesthesiologists-PS score ≤ 2 (Appendix III).
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Agrees not to have any additional weight loss interventional procedures, liposuction, or take any over the counter or prescription weight loss medication for 24 months following study enrollment.
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Have not taken any prescription or over the counter weight loss medications for at least 6 months and agrees not to utilize for 12 months following study enrollment.
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Be willing to cooperate with post-operative dietary recommendations and assessment tests.
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Reside within a reasonable distance from the Investigator's treating office (~50 miles) and able and willing to travel to the Investigator's office to complete all routine follow-up visits.
Exclusion Criteria:
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History of (or intra-operative evidence of) prior bariatric, gastric or esophageal surgery.
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Esophageal stricture or other anatomy and/or condition that could preclude passage of endolumenal instruments.
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Severe gastro-esophageal reflux disease (GERD), defined as symptoms that cause subject severe discomfort, compromise performance of daily activities, and/or condition is not entirely controlled with prescription drug therapy.
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Large hiatal hernia (>3 cm) by history or as determined by pre-randomization endoscopy.
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Pancreatic insufficiency/disease.
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Active gastric erosions or gastric/duodenal ulcer.
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History of gastroparesis or symptoms that would be suggestive of gastroparesis.
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Pregnancy or plans of pregnancy in the next 12 months.
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Immunosuppressive medications or systemic steroids (i.e., oral prednisone) within 1 month of Visit 1. Intranasal/inhaled steroids are acceptable.
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History of inflammatory disease of the GI tract; coagulation disorders; hepatic insufficiency or cirrhosis
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History or present use of insulin or insulin derivatives for treatment of diabetes
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Type II Diabetes Mellitus (as defined by HgbA1c >6.5%) for greater than 10 years at the time of enrollment
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Quit smoking within the last 6 months at time of enrollment or plans to quit smoking in the year after enrollment
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Portal hypertension and/or varices.
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Gastric outlet obstruction or stenosis.
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Significant abnormality identified during Visit 2 (randomization visit) with endoscopy revealing large hiatal hernia, gastric ulcer, gastric erosions, etc.
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Patient has a history of drug or alcohol abuse or positive at screening for drugs of abuse.
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Beck Depression Inventory (Short) Score ≥12 and/or uncontrolled depression after pre-enrollment psychological and medical assessment.
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Present or past history of psychosis, bipolar disease, or obsessive compulsive disorder after pre-enrollment history and medical /psychological assessment.
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Non-ambulatory or has significant impairment of mobility.
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Known hormonal or genetic cause for obesity with the exception of treated hypothyroidism.
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Participating in another clinical study.
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Is a relative of investigator or his/her staff, or is employed by investigator or institution involved in the study.
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Subjects with a personal history of allergic/anaphylactic reactions including hypersensitivity to the drugs or materials that will be utilized in the study procedure.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Scottsdale Healthcare | Scottsdale | Arizona | United States | 85258 |
| 2 | DeWitt Daughtry Family Department of Surgery University of Miami Miller School of Medicine | Miami | Florida | United States | 33166 |
| 3 | Hamilton Medical Center | Dalton | Georgia | United States | 30722 |
| 4 | NorthShore University HealthSystem | Evanston | Illinois | United States | 60201 |
| 5 | Crescent City Surgical Centre | Covington | Louisiana | United States | 70433 |
| 6 | Brigham & Women's Hospital | Boston | Massachusetts | United States | 02120 |
| 7 | University of MN, Fairview Health Services | Minneapolis | Minnesota | United States | 55455 |
| 8 | Saint Luke's Hospital | Kansas City | Missouri | United States | 64111 |
| 9 | Washington University School of Medicine | St. Louis | Missouri | United States | 63110 |
| 10 | Lexington Medical Center | West Columbia | South Carolina | United States | 29169 |
| 11 | Baptist Memorial | Memphis | Tennessee | United States | 38120 |
Sponsors and Collaborators
- USGI Medical
Investigators
- Principal Investigator: Tom Lavin, MD, Crescent City Surgical Center
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- G130163