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Single Anastomosis Duodenal Ileal Bypass (SADI) for Sleeve Revision (SADI)

Primary Purpose

Bariatric Surgery Candidate, Severe Obesity

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Single Anastomosis Duodenal Ileal Bypass (SADI)
Sponsored by
Kaiser Permanente
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bariatric Surgery Candidate focused on measuring weight loss failure, laparoscopic sleeve gastrectomy

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Body Mass Index (BMI) 35 - 39 kg/m2 with comorbid conditions; OR
  2. BMI 40+ kg/m2 with no comorbidities; AND
  3. having a previous laparoscopic sleeve gastrectomy (LGS); AND
  4. having lost less than 10% total weight loss with this LSG; AND
  5. being a Kaiser member at the time of surgery; AND
  6. being at least 18 years of age.

Exclusion Criteria:

  1. BMI less than 35 kg/m2; OR
  2. having a hiatal hernia; OR
  3. having severe Gastroesophageal Reflux Disease; OR
  4. having a primary bariatric procedure other than LSG; OR
  5. having already had a revisional bariatric procedure; OR
  6. being less than 18 years old.

Sites / Locations

  • Kaiser Permanente Southern California West Los Angeles Medical Center

Outcomes

Primary Outcome Measures

Percent Total Weight Loss (change in weight relative to baseline)
This is weight loss relative to the initial body weight at the time of surgery calculated as (weight at surgery - weight at follow-up)/weight at surgery. This is already a change score.

Secondary Outcome Measures

Full Information

First Posted
November 7, 2019
Last Updated
March 20, 2023
Sponsor
Kaiser Permanente
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1. Study Identification

Unique Protocol Identification Number
NCT04165694
Brief Title
Single Anastomosis Duodenal Ileal Bypass (SADI) for Sleeve Revision
Acronym
SADI
Official Title
Single Anastomosis Duodenal Ileal Bypass (SADI) as a Second Stage for Sleeve Gastrectomy Weight Loss Failure
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 15, 2019 (Actual)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
December 31, 2030 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kaiser Permanente

4. Oversight

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

5. Study Description

Brief Summary
The goal of this study is two part: 1) to add to the literature which is still somewhat sparse with numbers of patients undergoing the Single Anastomosis Duodenal Ileal Bypass (SADI) as a revision for laparoscopic sleeve gastrectomy (LSG) and 2) to have a treatment option for our Kaiser Permanente patients who seek additional assistance after a LSG with persistent morbid obesity and the comorbidities that come with it.
Detailed Description
Patients will be recruited during 10/15/2019 through 12/31/2022 with the following inclusion criteria: 1) body mass index (BMI) 35 - 39 kg/m2 with comorbid conditions; 2) BMI 40+ kg/m2 with no comorbidities; 3) having a previous LGS; 4) having lost less than 10% total weight loss with this LSG; 5) being a Kaiser member at the time of surgery; and 6) being at least 18 years of age. Exclusion criteria will include: 1) BMI less than 35; 2) having a hiatal hernia; 3) having severe Gastroesophageal Reflux Disease; 4) having a primary bariatric procedure other than LSG; 5) having already had a revisional bariatric procedure; and 6) being less than 18 years old. Age range for participants will be 18 - 100 years old. We will recruit 50 patients. Revisional procedures for weight regain are PART OF USUAL CARE at Kaiser Permanente Southern California. However SADI is a type of revisional procedure that is still considered experimental. This procedure has a single surgical anastomosis. It has a restrictive component when reducing the greater curvature of the stomach, but specially a malabsorptive component, as the common channel is also reduced. The objective of this surgical technique is to lessen the intestinal loop where nutrients are absorbed. It was part of a more extreme procedure, that is currently standard of care, called the Duodenal Switch (DS). The DS procedure which is PART OF USUAL CARE results in very successful massive weight loss however, it also has severe complications especially vitamin deficiencies. The SADI procedure is thought to confer the same weight loss benefits of the DS but without the severe complications. This has not been tested systematically. These eligibility criteria will be verified by the bariatric surgeon who is doing the consult for a revisional procedure AS PART OF USUAL CARE. This will entail the surgeon looking in the electronic medical record before meeting with the patient. However, this review of the medical record before surgical consult is PART OF USUAL CARE. All data collection and study follow-up visits are PART OF USUAL CARE for bariatric patients at Kaiser Permanente Southern California. THIS INCLUDES PATIENTS WHO RECEIVE REVISIONAL SURGERY. The only part of the study that is not usual care is the surgical procedure itself. The patients enrolled in the proposed study will receive the following visits AS PART OF USUAL CARE: Surgical consult 2 - 6 weeks before surgery at which point the patients will be offered the SADI procedure and consent will be done by the surgeon doing the consult in person in the surgeon's office in the Department of Surgery at the West Los Angeles Medical Center. Visit with bariatric physician 7 - 10 days before surgery to go over laboratory values and to insure instructions for surgical preparation were followed. Visit with surgeon and bariatric physician 7 - 10 days after surgery. Visit with bariatric physician 4 - 6 weeks after surgery. Visit 6 months after surgery with surgeon, bariatric physician, and other te am members as necessary (i.e. nutritionist or social worker). Visit 12 months after surgery with surgeon, bariatric physician, and other team members as necessary (i.e. nutritionist or social worker). Annual phone calls at years 1, 2 and 3 after surgery with bariatric care manager to monitor laboratory measures, weight loss, and complications. All data to evaluate the effectiveness of SADI will be abstracted from the electronic medical record, These measures are taken from the patients as PART OF US UAL CARE. There are no specific measures added to usual care for the SADI procedure. We already have a protocol for the DS procedure. These data will include weight, height, laboratory results, diagnoses, utiliza tion of services, and pharmacy records. No questionnaires will be used in this study. For each patient, data will be abstracted for 12 months before surgery and up to 3 years after surgery. No questionnaires will be administered. The primary outcome for the study will be percent total weight loss at 3 years calculated as (weight at surgery - weight at 3 years)/weight at surgery. Data will be analyzed using linear regression to predict what factors at baseline such as disease burden, gender, age, race ethnicity, and BMI predict percent total weight loss at 3 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bariatric Surgery Candidate, Severe Obesity
Keywords
weight loss failure, laparoscopic sleeve gastrectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
The study is a pre-/post-test prospective intervention.
Masking
None (Open Label)
Allocation
N/A
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Single Anastomosis Duodenal Ileal Bypass (SADI)
Intervention Description
The purpose of the research is to study additional weight loss and resolution of comorbidities in patients who undergo revision of their sleeve gastrectomy to a Single Anastomosis Duodenal Ileal bypass (SADI). The sleeve gastrectomy which you have already undergone is now the most common bariatric procedure performed. This operation was part of a 2-stage operation known a Duodenal Switch (DS) which was a sleeve gastrectomy followed by a long bypass of the intestine that involved 2 connections. This operation has many complications such as vitamin deficiencies and potential malnutrition. The SADI procedure is a version of the DS that bypasses less of the intestine and one less connection of the small bowel.
Primary Outcome Measure Information:
Title
Percent Total Weight Loss (change in weight relative to baseline)
Description
This is weight loss relative to the initial body weight at the time of surgery calculated as (weight at surgery - weight at follow-up)/weight at surgery. This is already a change score.
Time Frame
3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Body Mass Index (BMI) 35 - 39 kg/m2 with comorbid conditions; OR BMI 40+ kg/m2 with no comorbidities; AND having a previous laparoscopic sleeve gastrectomy (LGS); AND having lost less than 10% total weight loss with this LSG; AND being a Kaiser member at the time of surgery; AND being at least 18 years of age. Exclusion Criteria: BMI less than 35 kg/m2; OR having a hiatal hernia; OR having severe Gastroesophageal Reflux Disease; OR having a primary bariatric procedure other than LSG; OR having already had a revisional bariatric procedure; OR being less than 18 years old.
Facility Information:
Facility Name
Kaiser Permanente Southern California West Los Angeles Medical Center
City
Los Angeles
State/Province
California
ZIP/Postal Code
90034
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Single Anastomosis Duodenal Ileal Bypass (SADI) for Sleeve Revision

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