Gastric Electrical Stimulation (GES) for the Treatment of Obesity

NCT01823705 | Completed DMC

• 1 other identifier: Exilis-1
• Study Type: interventional
• Target: 32
• Locations: 2 countries
• Sites: 4

Brief Summary

The purpose of this feasibility study is to provide safety data on the implantable Exilis gastric electrical stimulation (GES) system, to individually adjust stimulation parameters to levels that are comfortable for implanted subjects during chronic daily treatment, and to collect data on acute gastrointestinal function and food intake responses to GES during in-clinic testing.

Conditions

Obesity

Outcome Measures

Primary Outcomes (2)

• First-in-human experience with the Exilis System, including initial clinical feasibility and safety data, as well as data on device performance (e.g., recharge durations and intervals) and use conditions (e.g., stimulation amplitudes, lead impedances).

  Once adjudicated by the Adverse Events Advisory Committee (AEAC), all adverse events recorded during the study were tabulated and summarized by seriousness, intensity, and related. Device performance and use conditions where characterized by collecting data on amplitude settings and lead impedance recorded during device interrogations and conducted at each clinic visits. The data will be tabulated and summarized using descriptive statistics, but no hypotheses tests were pre-specified

  Duration of study

• To gain an understanding of what sensations, if any, subjects feel during GES treatment, and what level and type of sensations subjects find acceptable and comfortable during chronic daily treatment.

  In-clinic sensory testing and telephone follow-up were collected during Amplitude Titration phase and will be summarized. No formal hypothesis testing were pre-specified. Fourt separate visits were conducted approximately weekly during the titration phase. The testing procedure was expected to be repeated twice during each visits; once in a fasted state and once in a fed state. Subjects were asked to rate exposure sensitive from 0 (none) to 5 (intense)

  4 weeks

Secondary Outcomes (5)

• Change in gastric emptying time across a pair of in-clinic measurements made with and without GES.

  Screening, Week 26 and Week 52

• Change in whether GES delivered with the Exilis System suppresses post-meal gastric contractile activity

  8 and 10 weeks

• Change in post-meal plasma glucose and insulin concentrations

  Baseline and 6 months

• Changes in coloric intake during a standardized ad libitum solid meal consumed in a controlled setting

  8 and 10 weeks

• Change in physiological parameters, medication usage, and psychometric assessment scores that occur during chronic daily GES treatment with the Exilis System.

  Study duration

Study Arms (1)

Gastric Electrical Stimulation (GES)

EXPERIMENTAL

Gastric Electrical Stimulation (GES) therapy for the treatment of obesity.

Device: Exilis Implantable Gastric Electrical Stimulation (GES)

Interventions

Exilis Implantable Gastric Electrical Stimulation (GES) DEVICE

Also known as: Exilis Implantable Gastric Electrical Stimulation

Gastric Electrical Stimulation (GES)

Eligibility Criteria

• Age: 21 Years - 64 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Adults ages 21-64 with BMI of 40-45 kg/m\^2 or BMI 35-39.9 kg/m\^2 with at least one obesity-related comorbidity, who have failed prior non-surgical weight loss attempts, and have been within 5% of their current weight for at least one year.
• If diabetic, subject has non-insulin-dependent type 2 diabetes mellitus diagnosed within the last 7 years, and has an HbA1c level less than 8%.
• If female and of child-bearing age, subject is not pregnant or lactating and is willing to use effective contraception for the duration of the study.
• Subject is willing and able to complete scheduled study visits, complete on-line lifestyle educational modules, and complete required procedures.

You may not qualify if:

• Subject has a history of medical, surgical, or psychiatric conditions that, in the opinion of the Investigators, would limit study participation or contraindicate implantation of the Exilis GES system. Examples includes cardiac abnormalities contraindicating surgical anesthesia, prior gastrointestinal surgery, gastrointestinal motility disorders, inflammatory bowel disease, a history of eating disorders, anticipated future need for magnetic resonance imaging, or allergies to food ingredients in study test meals.

Sponsors & Collaborators

• Medtronic Corporate Technologies and New Ventures: lead

Study Sites (4)

Unknown Facility

Scottsdale, Arizona, 85258, United States

Location

Unknown Facility

Louisville, Kentucky, 40202, United States

Location

Unknown Facility

Nashville, Tennessee, 37232, United States

Location

Unknown Facility

Maastricht, 6229, Netherlands

Location

MeSH Terms

Conditions

Obesity

Condition Hierarchy (Ancestors)

Overweight; Overnutrition; Nutrition Disorders; Nutritional and Metabolic Diseases; Body Weight; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 26, 2013
• First Posted: April 4, 2013
• Study Start: March 29, 2013
• Primary Completion: January 13, 2017
• Study Completion: January 13, 2017
• Last Updated: October 2, 2018

Record last verified: 2018-09

Data Sharing

• IPD Sharing: Will not share

Locations

US (3); NL (1)