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Management of Sleeve Gastrectomy Failure Using Single-anastomosis Metabolic Surgery

Primary Purpose

Obesity, Obesity, Morbid

Status
Not yet recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Standard duodenal switch
Single-anastomosis duodenal switch
Sponsored by
Laval University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Bariatric surgery

Eligibility Criteria

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

Inclusion Criteria:

  • had sleeve gastrectomy a minimum of 18 months before
  • still meet the NIH criteria for bariatric surgery (BMI≥35kg/m2 with major comorbidities or BMI≥40kg/m2) or patients with EWL<50% or significant weight regain (≥20%EWL)

Exclusion Criteria:

  • general contra-indication for bariatric surgery
  • BMI<35kg/m2
  • pregnancy
  • cirrhosis
  • abnormal bowel habits including irritable bowel syndrome and inflammatory bowel disease

Sites / Locations

  • Institut Universitaire de Cardiologie et de Pneumologie de Québec

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

biliopancreatic diversion with duodenal switch

Single-anastomosis duodeno-ileal anastomosis

Arm Description

Patient randomized for a the standard duodenal switch as second stage surgery after a sleeve gastrectomy (100cm common channel and 150cm alimentary limb)

Patient randomized for a single-anastomosis duodeno-ileal anastomosis as second stage surgery after a sleeve gastrectomy (250cm common channel)

Outcomes

Primary Outcome Measures

Excess weight loss
Percentage of excess weight loss mobilized in response to surgery

Secondary Outcome Measures

Peroperative complications
Complications graded with Clavien classification
Risk of malnutrition
Risk of malnutrition assessed through measurement of its risk being mild (albumin<35g\L), moderate (albumin<30g/L) or severe (albumin<25g/L)
Change in quality of life (SF-36)
36-item short form survey evaluating quality of life on a scale form 0 to 100
Change in quality of life (BAROS)
Bariatric Analyses and Reporting Outcomes System score form -7 to 9
Change in quality of life (QLaval)
Laval questionnaire evaluating quality of life on 6 aspects on a scale from 0 to 7
Gastro-intestinal side effects
Evaluation of gastro-intestinal side effects with the Gastro-Intestinal Quality of Life Index from 0 to 144
Change in nutritional status (calcium)
Change in nutritional status based on blood analysis of calcium (mmol/L)
Change in nutritional status (ferritin)
Change in nutritional status based on blood analysis of ferritin (ug/L)
Change in nutritional status (TIBC)
Change in nutritional status based on blood analysis of TIBC (umol/L)
Change in nutritional status (iron)
Change in nutritional status based on blood analysis of iron (umol/L)
Change in nutritional status (prealbumin)
Change in nutritional status based on blood analysis of prealbumin (g/L)
Change in nutritional status (transferrin)
Change in nutritional status based on blood analysis transferrin (g/L)
Change in nutritional status (vitamin A)
Change in nutritional status based on blood analysis of vitamin A (umol/L)
Change in nutritional status (vitamin D3)
Change in nutritional status based on blood analysis of vitamin D3 (nmol/L)
Change in nutritional status (parathormone)
Change in nutritional status based on blood analysis parathormone (ng/L)
Change in food intake
Evaluation of the change in food intake using a web-based food frequency questionnaire (kcal/day)
Change in eating behavior
Change of eating behavior using the Three-Factor Eating Questionnaire evaluating cognitive restraint of eating on a scale from 0 to 20, disinhibition on a scale from 0 to 16 and hunger on a scale from 0 to 15
Change in food addiction
Change of eating behavior using the Yale Food Addiction Scale that includes a "symptom count" scale from 0 to 7 reflecting the number of addiction-like criteria endorsed and a dichotomous evaluation that indicates whether a threshold of three or more "symptoms" plus clinically significant impairment or distress has been met
Change in binge eating behavior
Change of eating behavior using the Binge Eating scale from 0 to 46
Evolution of obesity related diseases
Remission rate for comorbidities, including T2D, hypertension, dyslipidemia, sleep apnea according to the ASMBS definition of outcomes reporting

Full Information

First Posted
January 25, 2022
Last Updated
February 7, 2022
Sponsor
Laval University
Collaborators
Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
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1. Study Identification

Unique Protocol Identification Number
NCT05242835
Brief Title
Management of Sleeve Gastrectomy Failure Using Single-anastomosis Metabolic Surgery
Official Title
Management of Sleeve Gastrectomy Failure Using Single-anastomosis Metabolic Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2022 (Anticipated)
Primary Completion Date
January 2027 (Anticipated)
Study Completion Date
March 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Laval University
Collaborators
Institut universitaire de cardiologie et de pneumologie de Québec, University Laval

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Sleeve gastrectomy (SG) has become the most commonly performed weight loss surgery, accounting for 60% of all bariatric operations worldwide. While technically easier with less side-effects and nutritional risks than other operations, SG is also associated with a higher risk of failure (20 to 40%). In such case, the most effective option consists in adding an intestinal bypass called the Biliopancreatic Diversion with Duodenal Switch (BPD-DS). This surgery is, however, technically challenging and yields a significant risk of complications, nutritional deficiencies or gastro-intestinal side-effects. Recently, a simplified version of the Standard DS, called Single-Anastomosis Duodenoileal Switch (SADI-S) was endorsed by surgical societies as one of the approved bariatric procedures. There is currently no prospective or randomized data to support the effectiveness of this new procedure, especially as a revisional approach. The Overall Objective of this randomized controlled trial project is to establish the clinical benefits of the SADI-S as a revisional surgery after SG, while also considering critical issues related to sex and gender. The investigator Overall Hypothesis is that the SADI-S represents a relevant revisional option for weight loss and metabolic recovery in women and men suffering from severe obesity who had a previous SG. The investigator propose to address the following research question. Research Question: What are the clinical effects of SADI-S compared to standard DS when used as a revisional procedure after SG, in patients with obesity? Participants who need revisional surgery after SG will be enrolled in a prospective, randomized, double-blind (patient-evaluator), non-inferiority trial comparing SADI-S vs DS. The primary outcome will be 12-month excess weight loss. Secondary outcomes will be perioperative complications, risk of malnutrition, quality of life and gastrointestinal side effects. The investigator hypothesize that SADI-S offers similar weight loss compared to standard DS, but a lower risk of complications and nutritional deficiencies. With the increase in the number of bariatric operations performed worldwide and the recent endorsement of the SADI-S as a regular procedure, reliable clinical data are urgently needed. The present proposal will directly address this knowledge gap.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Obesity, Morbid
Keywords
Bariatric surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
151 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
biliopancreatic diversion with duodenal switch
Arm Type
Active Comparator
Arm Description
Patient randomized for a the standard duodenal switch as second stage surgery after a sleeve gastrectomy (100cm common channel and 150cm alimentary limb)
Arm Title
Single-anastomosis duodeno-ileal anastomosis
Arm Type
Experimental
Arm Description
Patient randomized for a single-anastomosis duodeno-ileal anastomosis as second stage surgery after a sleeve gastrectomy (250cm common channel)
Intervention Type
Procedure
Intervention Name(s)
Standard duodenal switch
Other Intervention Name(s)
BPD-DS
Intervention Description
Standard duodenal switch as second stage surgery after a sleeve gastrectomy (100cm common channel and 150cm alimentary limb)
Intervention Type
Procedure
Intervention Name(s)
Single-anastomosis duodenal switch
Other Intervention Name(s)
SADI
Intervention Description
Single-anastomosis duodeno-ileal anastomosis as second stage surgery after a sleeve gastrectomy (250cm common channel)
Primary Outcome Measure Information:
Title
Excess weight loss
Description
Percentage of excess weight loss mobilized in response to surgery
Time Frame
12 month
Secondary Outcome Measure Information:
Title
Peroperative complications
Description
Complications graded with Clavien classification
Time Frame
from baseline up to 60 months
Title
Risk of malnutrition
Description
Risk of malnutrition assessed through measurement of its risk being mild (albumin<35g\L), moderate (albumin<30g/L) or severe (albumin<25g/L)
Time Frame
from baseline to 60 months
Title
Change in quality of life (SF-36)
Description
36-item short form survey evaluating quality of life on a scale form 0 to 100
Time Frame
from baseline to 60 months
Title
Change in quality of life (BAROS)
Description
Bariatric Analyses and Reporting Outcomes System score form -7 to 9
Time Frame
from baseline to 60 months
Title
Change in quality of life (QLaval)
Description
Laval questionnaire evaluating quality of life on 6 aspects on a scale from 0 to 7
Time Frame
from baseline to 60 months
Title
Gastro-intestinal side effects
Description
Evaluation of gastro-intestinal side effects with the Gastro-Intestinal Quality of Life Index from 0 to 144
Time Frame
from baseline to 60 months
Title
Change in nutritional status (calcium)
Description
Change in nutritional status based on blood analysis of calcium (mmol/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (ferritin)
Description
Change in nutritional status based on blood analysis of ferritin (ug/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (TIBC)
Description
Change in nutritional status based on blood analysis of TIBC (umol/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (iron)
Description
Change in nutritional status based on blood analysis of iron (umol/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (prealbumin)
Description
Change in nutritional status based on blood analysis of prealbumin (g/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (transferrin)
Description
Change in nutritional status based on blood analysis transferrin (g/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (vitamin A)
Description
Change in nutritional status based on blood analysis of vitamin A (umol/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (vitamin D3)
Description
Change in nutritional status based on blood analysis of vitamin D3 (nmol/L)
Time Frame
from baseline to 60 months
Title
Change in nutritional status (parathormone)
Description
Change in nutritional status based on blood analysis parathormone (ng/L)
Time Frame
from baseline to 60 months
Title
Change in food intake
Description
Evaluation of the change in food intake using a web-based food frequency questionnaire (kcal/day)
Time Frame
from baseline to 60 months
Title
Change in eating behavior
Description
Change of eating behavior using the Three-Factor Eating Questionnaire evaluating cognitive restraint of eating on a scale from 0 to 20, disinhibition on a scale from 0 to 16 and hunger on a scale from 0 to 15
Time Frame
from baseline to 60 months
Title
Change in food addiction
Description
Change of eating behavior using the Yale Food Addiction Scale that includes a "symptom count" scale from 0 to 7 reflecting the number of addiction-like criteria endorsed and a dichotomous evaluation that indicates whether a threshold of three or more "symptoms" plus clinically significant impairment or distress has been met
Time Frame
from baseline to 60 months
Title
Change in binge eating behavior
Description
Change of eating behavior using the Binge Eating scale from 0 to 46
Time Frame
from baseline to 60 months
Title
Evolution of obesity related diseases
Description
Remission rate for comorbidities, including T2D, hypertension, dyslipidemia, sleep apnea according to the ASMBS definition of outcomes reporting
Time Frame
from baseline to 60 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: had sleeve gastrectomy a minimum of 18 months before still meet the NIH criteria for bariatric surgery (BMI≥35kg/m2 with major comorbidities or BMI≥40kg/m2) or patients with EWL<50% or significant weight regain (≥20%EWL) Exclusion Criteria: general contra-indication for bariatric surgery BMI<35kg/m2 pregnancy cirrhosis abnormal bowel habits including irritable bowel syndrome and inflammatory bowel disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mélanie Nadeau, MSc
Phone
418-656-8711
Ext
3490
Email
melanie.nadeau@criucpq.ulaval.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Suzy Laroche
Phone
418-656-8711
Ext
3841
Email
suzy_laroche@ssss.gouv.qc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Laurent Biertho, MD
Organizational Affiliation
Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut Universitaire de Cardiologie et de Pneumologie de Québec
City
Quebec City
State/Province
Quebec
ZIP/Postal Code
G1V 4G5
Country
Canada

12. IPD Sharing Statement

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Management of Sleeve Gastrectomy Failure Using Single-anastomosis Metabolic Surgery

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