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ENDOBARRIER® and Conventional Therapy in the Management of Metabolic Syndrome in Obese Patients (ENDOMETAB)

Primary Purpose

Metabolic Syndrome

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
ENDOBARRIER®
Sponsored by
University Hospital, Lille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome focused on measuring Obesity, Metabolic Syndrome, ENDOBARRIER®

Eligibility Criteria

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

Inclusion Criteria:

  • Clinical diagnosis of Metabolic Syndrome defined by the presence of at least 3 of the 5 factors identified in the harmonization of the definition of metabolic syndrome by the International Diabetes Federation, the American Heart Association and the National Heart, Lung and Blood Institute
  • BMI > 30 kg/m2
  • The subject must be a candidate for general anesthesia
  • The subject must be able to understand the options to comply with the requirement of each intervention program.
  • Non-pregnant female patients must agree to use a reliable method of contraception for 2 years

Exclusion Criteria:

  • Contraindications from the notice of ENDOBARRIER device

Sites / Locations

  • Hôpital Avicenne
  • Hopital Ambroise Pare (Ap-Hp)
  • Hopital Louis Mourier
  • University Hospital Lille
  • Hospice civils de Lyon
  • Assistance Publique des Hôpitaux de Marseille
  • Centre Hospitalier Universitaire
  • Centre Hospitalier Universitaire
  • Nouvel Hôpital Civil
  • Hopital Larrey- Chu

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Conventional medical therapy

ENDOBARRIER®

Arm Description

Conventional medical therapy is defined as the use of the latest lifestyle guidelines to optimize weight loss and glycaemic management, frequent home monitoring/titration strategies, use of latest approved drug therapy for treatment of hyperglycaemia and restoration of pancreatic B cell function, also for dyslipidemia and hypertension in addition to regular follow-up visits to a medical doctor from a multidisciplinary team

The interventional therapy will be the device ENDOBARRIER® over conventional medical therapy

Outcomes

Primary Outcome Measures

Frequency of patients without Metabolic Syndrome
The primary end point will be the rate of resolution of Metabolic Syndrome at 1 year as measured by frequency of patients without MS at 12 months.

Secondary Outcome Measures

The level of insulin resistance
Changed in cardiovascular risk assessed by Framingham Risk Score
Changed in quality of life
Rate of adverse events
The cost-benefit ratio for each group
The cost-benefit ratio for each group by evaluating the medical costs in each arm
Changed in blood pressure
Changed in specific metabolic syndrome parameters such blood pressure
Changed in blood sugar
Changed in blood sugar
Changed in triglycerides
Changed in triglycerides
Changed in HDL
Changed in HDL
Changed in waist circumference
Changed in waist circumference

Full Information

First Posted
September 18, 2014
Last Updated
May 15, 2018
Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France
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1. Study Identification

Unique Protocol Identification Number
NCT02297555
Brief Title
ENDOBARRIER® and Conventional Therapy in the Management of Metabolic Syndrome in Obese Patients
Acronym
ENDOMETAB
Official Title
ENDOBARRIER® vs Conventional Therapy in the Management of Metabolic Syndrome in Obese Patients. Medico-economic Analysis as Part of a Randomized Controlled Multicenter Trial - ENDOMETAB
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Terminated
Study Start Date
April 2014 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
October 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Obesity and metabolic syndrome (MS) are closely interrelated leading to increased mortality, mainly due to cardiovascular disease. In addition, some cancers are much higher when obesity is associated with metabolic syndrome. Bariatric surgery allows significant and sustained weight loss with marked improvement of MS. Considered too invasive, surgery is proposed to a small proportion of patients who could theoretically benefit. The ENDOBARRIER® device implanted endoscopically is an innovative approach developed for management of obesity in the non-surgical manner with benefits for improvement in MS already reported in literature.
Detailed Description
Obesity, defined as a body mass index (BMI) over 30 kg / m², has now affected more than 14% of the French population. This condition is associated with several co-morbidities, and increased mortality, mainly due to cardiovascular disease and some cancers. These risks are much higher when obesity is associated with metabolic syndrome. Conventional medical care for metabolic syndrome, even conducted by multidisciplinary teams combining dietary advice, physical activity and psychological treatment offers only limited results, both in weight reduction and comorbidities. Bariatric surgery allows however a significant and sustained weight loss in the majority of cases, and a decrease in the frequency and severity of co-morbidities, including type 2 diabetes, and decreased mortality including cardiovascular. Considered too invasive by many practitioners and patients, surgery is therefore proposed to a small proportion of patients who could theoretically benefit. The results of surgery have, however, validated the principle of the interventional treatment of obesity and its metabolic complications. Different techniques that may replace surgery are currently being developed. Among these new approaches, the most successful is the device "endoluminal liner ENDOBARRIER®" (GI Dynamics ™, Boston, USA). The ENDOBARRIER® device could represent a major innovation in the non-surgical management of obesity. The benefits of installing the device on the morbidity associated with obesity are reported in the literature: impact on hypertension, diabetes, dyslipidemia and metabolic syndrome as such. This trial will compare in a randomized study the results, tolerance and cost of the interventional therapy with the device ENDOBARRIER® over conventional therapy in French patients with obesity and metabolic syndrome, with or without diabetes. The evaluation of the cost-effectiveness of this device will clarify its role in the strategy for the management of obesity and its comorbidities.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome
Keywords
Obesity, Metabolic Syndrome, ENDOBARRIER®

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
82 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conventional medical therapy
Arm Type
No Intervention
Arm Description
Conventional medical therapy is defined as the use of the latest lifestyle guidelines to optimize weight loss and glycaemic management, frequent home monitoring/titration strategies, use of latest approved drug therapy for treatment of hyperglycaemia and restoration of pancreatic B cell function, also for dyslipidemia and hypertension in addition to regular follow-up visits to a medical doctor from a multidisciplinary team
Arm Title
ENDOBARRIER®
Arm Type
Experimental
Arm Description
The interventional therapy will be the device ENDOBARRIER® over conventional medical therapy
Intervention Type
Device
Intervention Name(s)
ENDOBARRIER®
Intervention Description
This medical device consists of a tube (impermeable fluoropolymer) inserted endoscopically and secured by hooks in the wall of the duodenal bulb. From the anchor site, this duodeno-jejunal sheath covers 60 cm in the small intestine. It thus limits the contact of nutrients with digestive juices (bile and pancreatic juice) and initial absorption, at least in part mimicking duodenal exclusion of the gastric bypass, one of the techniques of bariatric surgery.
Primary Outcome Measure Information:
Title
Frequency of patients without Metabolic Syndrome
Description
The primary end point will be the rate of resolution of Metabolic Syndrome at 1 year as measured by frequency of patients without MS at 12 months.
Time Frame
12 month
Secondary Outcome Measure Information:
Title
The level of insulin resistance
Time Frame
12 months, 24 months
Title
Changed in cardiovascular risk assessed by Framingham Risk Score
Time Frame
12 months, 24 months
Title
Changed in quality of life
Time Frame
12 months, 24 months
Title
Rate of adverse events
Time Frame
12 months, 24 months
Title
The cost-benefit ratio for each group
Description
The cost-benefit ratio for each group by evaluating the medical costs in each arm
Time Frame
12 months, 24 months
Title
Changed in blood pressure
Description
Changed in specific metabolic syndrome parameters such blood pressure
Time Frame
12 months, 24 months
Title
Changed in blood sugar
Description
Changed in blood sugar
Time Frame
12 months, 24 months
Title
Changed in triglycerides
Description
Changed in triglycerides
Time Frame
12 months, 24 months
Title
Changed in HDL
Description
Changed in HDL
Time Frame
12 months, 24 months
Title
Changed in waist circumference
Description
Changed in waist circumference
Time Frame
12 months, 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of Metabolic Syndrome defined by the presence of at least 3 of the 5 factors identified in the harmonization of the definition of metabolic syndrome by the International Diabetes Federation, the American Heart Association and the National Heart, Lung and Blood Institute BMI > 30 kg/m2 The subject must be a candidate for general anesthesia The subject must be able to understand the options to comply with the requirement of each intervention program. Non-pregnant female patients must agree to use a reliable method of contraception for 2 years Exclusion Criteria: Contraindications from the notice of ENDOBARRIER device
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
François PATTOU, Professor
Organizational Affiliation
University Hospital of Lille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Avicenne
City
Bobigny
Country
France
Facility Name
Hopital Ambroise Pare (Ap-Hp)
City
Boulogne Billancourt
Country
France
Facility Name
Hopital Louis Mourier
City
Colombes
Country
France
Facility Name
University Hospital Lille
City
Lille
ZIP/Postal Code
59000
Country
France
Facility Name
Hospice civils de Lyon
City
Lyon
Country
France
Facility Name
Assistance Publique des Hôpitaux de Marseille
City
Marseille
Country
France
Facility Name
Centre Hospitalier Universitaire
City
Montpellier
Country
France
Facility Name
Centre Hospitalier Universitaire
City
Nantes
Country
France
Facility Name
Nouvel Hôpital Civil
City
Strasbourg
Country
France
Facility Name
Hopital Larrey- Chu
City
Toulouse
Country
France

12. IPD Sharing Statement

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ENDOBARRIER® and Conventional Therapy in the Management of Metabolic Syndrome in Obese Patients

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