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Vagal Blocking for Obesity Control

Primary Purpose

Obesity

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Active, implantable, intra-abdominal vagal blocking medical device
Sponsored by
ReShape Lifesciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Obesity, Bariatric surgery, Excess weight loss, Vagus nerve, Vagal blocking, VBLOC(TM) therapy

Eligibility Criteria

25 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Body mass index (BMI) 35-50 +/- 10% inclusive
  • Failure to respond to diet/exercise program

Exclusion Criteria:

  • History of gastric resection or major upper-abdominal surgery (e.g. cholycystectomy, hysterectomy acceptable)
  • Current type 1 diabetes mellitus (DM) or poorly controlled type 2 DM
  • Reductions of more than 10% of body weight in the previous 12 months
  • Current medical condition that would make subject unfit for surgery under general anesthesia or that would be exacerbated by intentional weight loss

Sites / Locations

  • Flinders Medical Centre
  • Institute of Weight Control
  • Instituto Nacional de la Nutrición Salvador Zubiran (INNSZ)
  • National Center for Advanced Laparoscopic Surgery, St. Olavs University Hospital
  • University Hospital Basel, Department of Internal Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A

Arm Description

All study subjects will be implanted with the Maestro System, and all will receive VBLOC therapy.

Outcomes

Primary Outcome Measures

Excess weight loss (EWL)
Serious Adverse Events (SAE) and Unanticipated Adverse Device Effects (UADE)

Secondary Outcome Measures

Full Information

First Posted
November 8, 2007
Last Updated
February 1, 2012
Sponsor
ReShape Lifesciences
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1. Study Identification

Unique Protocol Identification Number
NCT00555958
Brief Title
Vagal Blocking for Obesity Control
Official Title
VBLOC™ Clinical Trial: Vagal Block for Obesity Control
Study Type
Interventional

2. Study Status

Record Verification Date
February 2012
Overall Recruitment Status
Unknown status
Study Start Date
November 2005 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ReShape Lifesciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To determine the safety, efficacy and treatment algorithm(s) of the Maestro System in causing weight loss in obese subjects - This study will provide feasibility data regarding the potential of intra-abdominal vagus nerve down-regulation/block in the treatment of obesity.
Detailed Description
The development of innovative, safe and effective therapeutic options for the treatment of obese patients is both desirable and necessary. Gastric bypass operations are usually effective both short- and long-term but are also not available to or desired by many obese people for a variety of reasons. Gastric banding procedures are also available but have been reported to be less effective than gastric bypass operations. Diets, exercise programs and pharmaceutical agents offer short-term effectiveness for some obese patients but are all too often ineffective in the long term. The ever increasing impact of obesity on morbidity, mortality and accelerating healthcare resource utilization in most developed countries is well documented. Activation and up-regulation of the efferent and afferent fibers of the intra-abdominal vagal nerve trunks is a pivotal physiological mechanism for food ingestion, mechanical processing, enzymatic digestion and calorie absorption. EnteroMedics' Maestro™ System is designed to take therapeutic benefit from these physiological principles by reversibly and controllably down-regulating/blocking both the anterior and posterior intra-abdominal vagal trunks in order to: (1) reduce food intake by reducing gastric volume; (2) initiate early and prolonged satiation by delaying gastric emptying; and, (3) decrease calorie absorption by down-regulating pancreatic exocrine secretion and digestion. This multi-modal mechanism is implemented in order achieve predictable and controllable loss of body weight. This is a prospective, open-label, multi-center, clinical trial with the subjects' baseline parameters as the control. Subjects implanted laparoscopically with the Maestro System were followed from 6-months to two years. Implantable components: two flexible leads (including one electrode each for the anterior and posterior intra-abdominal vagal nerve trunks) that are connected to an implantable neuroregulator placed subcutaneously on the abdominal wall below the costal margin (a minimum of two or three finger widths below), or a location determined by the surgeon and consistent with device operation. External components: For the Maestro System using a neuroregulator with an internal rechargeable battery: one mobile charger for the implanted neuroregulator, which is connected via a small, flexible cable to a cutaneous transmit coil that is positioned over the implanted neuroregulator when charging the device or determining the status of the device; a software program on a laptop computer that transmits information to the neuroregulator and uploads data from the neuroregulator, which is available to the clinician, allowing both change in treatment regimens and assessment of treatment compliance. For the Maestro System using a neuroregulator with no battery: one programmable, battery-powered ambulatory controller connected via a small, flexible cable to a cutaneous transmit coil that is positioned over the implanted neuroregulator to provide power for the device; a software program on a laptop computer that transmits information to and uploads data from the controller which is available to the clinician, allowing both change in treatment regimens and assessment of treatment compliance. The objectives of this trial are as follows: Determination of efficacy by quantification of excess body weight loss (EWL) at 4 and 12 weeks, and 6, 12, 24, 36, 48 and 60 months. Evaluation of safety through 4 and 12 weeks, and 6, 12, 24, 36, 48 and 60 months. Selection of effective daily treatment regimen(s).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
Obesity, Bariatric surgery, Excess weight loss, Vagus nerve, Vagal blocking, VBLOC(TM) therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
All study subjects will be implanted with the Maestro System, and all will receive VBLOC therapy.
Intervention Type
Device
Intervention Name(s)
Active, implantable, intra-abdominal vagal blocking medical device
Intervention Description
Intermittent, programmable, intra-abdominal vagal blocking
Primary Outcome Measure Information:
Title
Excess weight loss (EWL)
Time Frame
4 and 12 weeks, and 6, 12, 24, 36, 48 and 60 months
Title
Serious Adverse Events (SAE) and Unanticipated Adverse Device Effects (UADE)
Time Frame
4 and 12 weeks, and 6, 12, 24, 36, 48 and 60 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Body mass index (BMI) 35-50 +/- 10% inclusive Failure to respond to diet/exercise program Exclusion Criteria: History of gastric resection or major upper-abdominal surgery (e.g. cholycystectomy, hysterectomy acceptable) Current type 1 diabetes mellitus (DM) or poorly controlled type 2 DM Reductions of more than 10% of body weight in the previous 12 months Current medical condition that would make subject unfit for surgery under general anesthesia or that would be exacerbated by intentional weight loss
Facility Information:
Facility Name
Flinders Medical Centre
City
Bedford Park
State/Province
South Australia
ZIP/Postal Code
5042
Country
Australia
Facility Name
Institute of Weight Control
City
Sydney
ZIP/Postal Code
2153
Country
Australia
Facility Name
Instituto Nacional de la Nutrición Salvador Zubiran (INNSZ)
City
Mexico City
ZIP/Postal Code
14000
Country
Mexico
Facility Name
National Center for Advanced Laparoscopic Surgery, St. Olavs University Hospital
City
Trondheim
ZIP/Postal Code
7489
Country
Norway
Facility Name
University Hospital Basel, Department of Internal Medicine
City
Basel
ZIP/Postal Code
4031
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
23984050
Citation
Shikora S, Toouli J, Herrera MF, Kulseng B, Zulewski H, Brancatisano R, Kow L, Pantoja JP, Johnsen G, Brancatisano A, Tweden KS, Knudson MB, Billington CJ. Vagal blocking improves glycemic control and elevated blood pressure in obese subjects with type 2 diabetes mellitus. J Obes. 2013;2013:245683. doi: 10.1155/2013/245683. Epub 2013 Jul 30.
Results Reference
derived

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Vagal Blocking for Obesity Control

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