ESSENTIAL Trial™ Sham Cross-over

Completed · Not applicable · Has a placebo group

Conditions studied: Obesity

In brief

This is a multicenter, un-blinded, open label, pivotal supplemental study to G130163 intended to evaluate the safety and efficacy of treating previous sham subjects in the Essential pivotal trial (IDE#G130163) with the active treatment (the placement of g-Cath EZ suture anchors along with diet and exercise). Compliant sham subjects (those who attended all primary IDE follow-up visits AND who continue to meet eligibility criteria as described in this protocol) will be offered this active treatment after their 12 month unblinding visit in the Essential pivotal trial.

Key facts

Study ID

NCT02279420

Run by

USGI Medical

People needed

73

Starts

2015-01-05

Expected to finish

2016-09-30

Last updated by the study team

2017-05-12

Who can join

Age: 23 and older, up to 61. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Provide written informed consent.
• Potential subject was sham participant in the Essential pivotal trial
• Potential subject agrees to be compliant with study and has a documented history of compliance in pivotal study.
• Subjects between the ages of 23-61 years.
• 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/baseline.
• 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 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 (See Section 14)
• Absence of current severe systemic disease (including, but not limited to: coronary artery disease, chronic obstructive pulmonary disease, congestive heart failure, cancer, and chronic renal disease)
• Agrees not to undergo any additional weight loss interventional procedures or liposuction for 12 months following study enrollment.
• Agrees not to utilize any prescription or over the counter weight loss medications OR those that can suppress appetite/induce weight loss for 12 months following study enrollment (including all stimulant medication).
• Be willing to cooperate with post-operative dietary recommendations and assessment tests.
• Residing 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.

You may not qualify if…

• History of (or intra-operative evidence of) prior bariatric, gastric or esophageal surgery.
• Esophageal stricture or other anatomy and/or condition that could preclude passage of endolumenal instruments or procedure execution.
• 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 drug therapy.
• Large hiatal hernia (>3 cm) by history or as determined by pre-enrollment endoscopy.
• Pancreatic insufficiency/disease.
• History of gastroparesis or symptoms that would be suggestive of gastroparesis.
• Pregnancy or plans of pregnancy in the next 12 months.
• Immunosuppressive medications or systemic steroids (i.e., oral prednisone) within 1 month of Visit 1. Intranasal/inhaled steroids are acceptable.
• History of inflammatory disease of the GI tract; coagulation disorders; hepatic insufficiency or cirrhosis
• History or present use of insulin or insulin derivatives for treatment of diabetes
• Type II Diabetes Mellitus (as defined by HgbA1c >6.5%) for greater than 11 years at the time of enrollment
• If smoker, plans to quit smoking in the year after enrollment
• Portal hypertension and/or varices.
• Significant abnormality identified during Visit 2 (enrollment visit) with endoscopy revealing large hiatal hernia, gastric/duodenal ulcer, gastric erosions, gastric outlet obstruction or stenosis, etc.
• Patient has a history of drug or alcohol abuse or positive at screening for drugs of abuse.
• Present or past history of psychosis, bipolar disease, or obsessive compulsive disorder after pre-enrollment history and medical /psychological assessment
• Non-ambulatory or has significant impairment of mobility.
• Known hormonal or genetic cause for obesity including untreated hypothyroidism (TSH >5.0 U/ml).
• Participating in another clinical study except for Essential Study.
• Subjects with a personal history of allergic/anaphylactic reactions including hypersensitivity to the drugs or materials that will be utilized in the study procedure.

Where it is running

• Shea Campus -Scottsdale Healthcare — Scottsdale, Arizona, United States
• University of Miami Hospital — Miami, Florida, United States
• Hamilton Medical Center — Dalton, Georgia, United States
• Northshore/Evanston Hospital — Evanston, Illinois, United States
• Crescent City Surgical — Metairie, Louisiana, United States
• Brigham & Women's Hospital — Boston, Massachusetts, United States
• Fairview UMMC-University — Minneapolis, Minnesota, United States
• Saint Luke's Hospital — Kansas City, Missouri, United States
• WA University School of Medicine — St Louis, Missouri, United States
• Lexington Medical Center — West Columbia, South Carolina, United States
• Baptist Memorial Hospital — Memphis, Tennessee, United States

Full record on ClinicalTrials.gov

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