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Assessment of the Overstich Technique for the Management of Weight Regain After Gastric Bypass.

Primary Purpose

the Management of Weight Regain After Gastric Bypass by Endoscopic Suturing

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Regular endoscopy + endogastric suturing
Regular endoscopy
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for the Management of Weight Regain After Gastric Bypass by Endoscopic Suturing focused on measuring Obesity, Endogastric suturing, Jujenal anastomosis, weight regain

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age > 18 years
  • Surgical criteria: patient with bariatric surgery by gastric bypass since, at least, 24 months
  • Clinics criteria of weight regain or treatment failure:

    • Patient with weight regain> 5kg / m²
    • Patient with EWL (excess weight loss) <25% after 2 years of treatment.
  • Loss of early satiety (interrogation)
  • Patient with a compatible psychological and cognitive status with the study,
  • Patient agreeing to follow the procedures of the study and can participate at the follow-up study during 2 years
  • Subject with no rights from the national health insurance programme
  • Consent form signed

Exclusion criteria:

  • Pregnancy (plasma assay of beta-HCG positive)
  • Presence of cardiovascular, neurological, psychiatric, endocrine, renal, gastrointestinal or tumor comorbidities making irrelevant patient participation in the judgment of the investigator
  • Patient participating in another clinical study or participated in another study within the last 30 days or for which the annual compensation received exceeds € 4,500
  • Patient with a contre-indication to the achievement of surgery (fistula, ulceration, ...)

Sites / Locations

  • Louis Mourier Hospital
  • Lille Hospital
  • Montpellier Hospital
  • Nice Hospital
  • HEGP Hospital
  • Strasbourg Hospital
  • Villeurbanne clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Arm with Apollo Endosurgery OverStitch technical

Arm without Apollo Endosurgery OverStitch technical

Arm Description

Outcomes

Primary Outcome Measures

Weight loss assessment of Apollo Endosurgery OverStitch technical
The main objective is to compare the efficacy of endoscopic surgery Apollo Endosurgery OverStitch technical than the conventional non-interventional strategy in patients with weight regain after gastric bypass.Moreover, all of these patients will also benefit from the medical-nutritional usual care.

Secondary Outcome Measures

Comparison of both strategies on tolerance (adverse events and serious adverse events)
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on tolerance and safety related to obesity.
Comparison of both strategies on comorbidities
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on comorbidities related to obesity (type 2 diabetes, arterial hypertension, sleep apnea syndrome, ...).
Comparison of both strategies on quality of life
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on quality of life.
Comparison of both strategies on medico-economic impact (drugs fees, medical consultation fees..)
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on medico-economic impact of innovation. Moreover, a cost-effectiveness analysis will be performed at the end of this study.

Full Information

First Posted
January 16, 2014
Last Updated
September 1, 2021
Sponsor
University Hospital, Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT02048033
Brief Title
Assessment of the Overstich Technique for the Management of Weight Regain After Gastric Bypass.
Official Title
Medico-economic Evaluation of the Management of Weight Regain After Gastric Bypass by Gastrointestinal Narrowing of Jejunal Anastomosis by Endoscopic Suturing: Apollo Endosurgery OverStitch Technical
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Terminated
Why Stopped
Following the occurrence of four serious adverse events in the APOLLO group and after discussion with the investigator, we consider that this minimally invasive protocol causes an increased risk of morbidity and mortality.
Study Start Date
January 3, 2014 (Actual)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
April 11, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Prospective multicenters randomized study to compare the efficiency and the socioeconomic impact of the endoscopic management (Overstitch technique) of weight regain after gastric bypass surgery to non invasive treatment
Detailed Description
Nowadays morbid obesity (BMI ≥ 40kg/m²) is a major problem of public health in industrialized countries. About 500 000 patients would be affected by this disease in France in 2009. Prevalence of the morbid obesity raised from 0.3 % (± 0.1 %) of the population in 1997 to 1.1 % (± 0.1 %) in 2009 (Extrapolation of the data ObEpi on 2009 to the French population) (1). For this type of patient, the only long-term effective treatment recognized by the scientists is the bariatric surgery. (2-4) Roux and Y Gastric Bypass (GBP) is a consensual procedure, that has been described in the sixties, in this indication (approximately 11000 GBP performed in FRance in 2012 (5,6). This operation consists on the creation of a proximal gastric pouch (50 cc). A Roux and Y intestinal loop will be added to create a malabsorptive part. 60 to 80 % of excess weight loss described in the literature in the long-terms. Furthermore, improvement or remission of T2DM, sleep apnea syndrome, arterial hyperpressure, dyslipidemia) are emphasized in many trials (5, 7). However 15 to 20 % of the handled patients present a weight regain 5 years post surgery potentially explained by the dilation of the gastric pouch or the gastro jejunal anastomosis and thus a decrease of the restrictive effect. (8-11) To palliate this complication two solutions are described. (12-15; 19) The first one consists in a recalibration of the gastric poouch by surgical approachy. In this case, a ring of silicone or polypropylene can be positioned around the gastric pocket. Other possible solution is to redo a new gastrojejunostomy with a smaller size, by surgical access (laparotomy or laparoscopy). These interventions are very delicate because of important peritoneal adhesions and present a rate of significant morbidity especially if they are performed under laparotomy. The pure medical care does not allow long-term results stable. ²² A therapeutic dead end is reported often for this type of patient. A new possibility was recently described. (17-18) A recalibration can be realized by sutures performed under endoscopic approach at the level of the gastro jejunal anastomosis or from the gastric pouch by the APOLLO Endosurgery OverStitch. The digestive surgery by endoscopic way is rapidly expanding. The first results seem to be promising (resumed the weight loss) but owe to be estimated in a randomized study comparing this new process with the medical conventional treatment. A single-blind, randomized, forward-looking study, multicenter, comparative between two parallel groups of patients presenting a weight regain after GBP was thus organized. The main objective is to estimate the efficiency of the APOLLO Endosurgery OverStitch technique versus the non-interventional strategy. The secondary endpoints is to study the morbidity of the procedure, the evolution of quality of life of the patients, the medical economic impact of the innovation in 24 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
the Management of Weight Regain After Gastric Bypass by Endoscopic Suturing
Keywords
Obesity, Endogastric suturing, Jujenal anastomosis, weight regain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
74 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Arm with Apollo Endosurgery OverStitch technical
Arm Type
Active Comparator
Arm Title
Arm without Apollo Endosurgery OverStitch technical
Arm Type
Placebo Comparator
Intervention Type
Device
Intervention Name(s)
Regular endoscopy + endogastric suturing
Intervention Description
Patients will get the usual endoscopy used for diagnosis. In addition, they will receive an endoscopic surgery using the APOLLO Endosuregery technique. The Apollo Endosurgery OverStitch is an endoscopic equipment which involves the suturing by endogastric way to decrease the size of the anastomosis gastrojujenal or gastric pouch
Intervention Type
Diagnostic Test
Intervention Name(s)
Regular endoscopy
Intervention Description
Patients will get the usual endoscopy used for diagnosis.
Primary Outcome Measure Information:
Title
Weight loss assessment of Apollo Endosurgery OverStitch technical
Description
The main objective is to compare the efficacy of endoscopic surgery Apollo Endosurgery OverStitch technical than the conventional non-interventional strategy in patients with weight regain after gastric bypass.Moreover, all of these patients will also benefit from the medical-nutritional usual care.
Time Frame
At 12 and 24 months after surgery
Secondary Outcome Measure Information:
Title
Comparison of both strategies on tolerance (adverse events and serious adverse events)
Description
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on tolerance and safety related to obesity.
Time Frame
At 12 months after Baseline and at each visit
Title
Comparison of both strategies on comorbidities
Description
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on comorbidities related to obesity (type 2 diabetes, arterial hypertension, sleep apnea syndrome, ...).
Time Frame
At 12 months after Baseline and at each visit
Title
Comparison of both strategies on quality of life
Description
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on quality of life.
Time Frame
At 12 months after Baseline and at each visit
Title
Comparison of both strategies on medico-economic impact (drugs fees, medical consultation fees..)
Description
The secondary objectives of this study were to compare in real life these both strategies of the management of weight regain after gastric bypass on medico-economic impact of innovation. Moreover, a cost-effectiveness analysis will be performed at the end of this study.
Time Frame
At 12 months after Baseline and at each visit

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age > 18 years Surgical criteria: patient with bariatric surgery by gastric bypass since, at least, 24 months Clinics criteria of weight regain or treatment failure: Patient with weight regain> 5kg / m² Patient with EWL (excess weight loss) <25% after 2 years of treatment. Loss of early satiety (interrogation) Patient with a compatible psychological and cognitive status with the study, Patient agreeing to follow the procedures of the study and can participate at the follow-up study during 2 years Subject with no rights from the national health insurance programme Consent form signed Exclusion criteria: Pregnancy (plasma assay of beta-HCG positive) Presence of cardiovascular, neurological, psychiatric, endocrine, renal, gastrointestinal or tumor comorbidities making irrelevant patient participation in the judgment of the investigator Patient participating in another clinical study or participated in another study within the last 30 days or for which the annual compensation received exceeds € 4,500 Patient with a contre-indication to the achievement of surgery (fistula, ulceration, ...)
Facility Information:
Facility Name
Louis Mourier Hospital
City
Colombes
ZIP/Postal Code
92700
Country
France
Facility Name
Lille Hospital
City
Lille
Country
France
Facility Name
Montpellier Hospital
City
Montpellier
ZIP/Postal Code
34000
Country
France
Facility Name
Nice Hospital
City
Nice
ZIP/Postal Code
06000
Country
France
Facility Name
HEGP Hospital
City
Paris
ZIP/Postal Code
75015
Country
France
Facility Name
Strasbourg Hospital
City
Strasbourg
ZIP/Postal Code
67000
Country
France
Facility Name
Villeurbanne clinic
City
Villeurbanne
ZIP/Postal Code
69000
Country
France

12. IPD Sharing Statement

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Assessment of the Overstich Technique for the Management of Weight Regain After Gastric Bypass.

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