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Metabolic Effects of Bariatric Arterial Embolization vs Bariatric Surgery (BEOD)

Primary Purpose

Obesity, Type2diabetes, Bariatric Surgery Candidate

Status
Recruiting
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Roux-en-Y gastric By-pass (RYGB) surgery
Bariatric Arterial Embolization (BAE) procedure
Sponsored by
Universidade Nova de Lisboa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring bariatric surgery, embolization, intensive medical therapy, BMI, glycemia

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: criteria: Is the candidate for general anesthesia. Body Mass Index (BMI) between 33 and 43 Kg/m2 Patients have a biochemical evidence of Type 2 Diabetes Mellitus (DMT2) confirmed by American Diabetes Association (ADA) criteria: 3.1) treated - HbA1c 7,1%; 3.2) If untreated- fasting 2-hour plasma glucose level of 200 mg/dL during an oral glucose tolerance test and a HbA1c of 7,1%. Willing, able, and mentally competent to provide written informed consent. Able o understand the options and to comply with the requirements of each program. Have a negative urine pregnancy test at screening and baseline visits (prior surgery and Embolization) for women of childbearing potential. Female patients must agree to use reliable method of contraception for 2 years. Exclusion Criteria: Prior bariatric surgery of any kind. Prior complex abdominal surgery including splenectomy, upper GI, anti-reflux surgery and trauma. Abdominal, thoracic, pelvic and/or obstetric-gynaecologic surgery within 3 months or at the discretion of the surgery. Cardiovascular conditions including uncompensated congestive heart failure, dysrhythmia, history of stroke, or uncontrolled hypertension (defined as medically treated with the mean of 3 separate measurements systolic blood pressure (SBP)> 180 mmHg or diastolic blood pressure (DBP) >110mmHg). Patients with coronary artery disease (CAD) that have been successfully treated with coronary artery by-pass graft (CABG) or percutaneous coronary intervention (PCI) or are 1 year after implantation of drug eluting stent and have no evidence of active ischemia are eligible. Known history of chronic liver disease (except for NAFLD/NASH), hepatitis, positive serologic test result for hepatitis B surface antigen and/or hepatitis C antibody, alpha-1-antitrypsin deficiency. Gastrointestinal disorders including a known history of celiac disease and/or other malabsorptive disorders or inflammatory bowel disease (Chron's disease or ulcerative colitis). Psychiatric disorders including dementia, active psychosis, severe depression requiring >2 medications, history of suicide attempts, alcohol or drugs abuse with previous 12months. Pregnancy. Malignancy within 5 years (except squamous cell and basal cell cancer of skin). Anaemia defined as haemoglobin less than 9 in females and 10 in males. Any medical condition requiring anticoagulation therapy that cannot be temporarily discontinued for surgical or embolic approach. Any condition or major illness that, in the investigator's judgment, places the subject at undue risk by participating in the study. Use of investigational therapy or participation in any other clinical trial within 12 weeks prior to signing the informed consent form. Severe pulmonary disease. American Society of Anesthesiologists (ASA) physical status class IV or higher. History of allergy to iodinated contrast media

Sites / Locations

  • Cruz Vermelha HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Roux-en-Y gastric By-pass (RYGB)

Bariatric Arterial Embolization (BAE)

Arm Description

RYGB procedure requires 1-2 hours of operating time and two to three days length of hospital stay. Use the Kit-RYGB by J& company.

Embosphere Microspheres (EM) are designed to offer controlled, target embolization. BAE procedure requires 1hour of operating time and one day length of hospital stay. Use the Kit by Merit MedicalCompany.

Outcomes

Primary Outcome Measures

Number of participants with glycated haemoglobin < 6%
The primary outcome of the study will be a level of glycated haemoglobin of 6.0% or less without the use of diabetes medications.

Secondary Outcome Measures

Determination of glycemic level (mg/dL)
Measures of glycemic control by evaluating glycemic level at fast in the blood in mg/dL. less than 126mg/dL will represent a good glycemic control
Weight evaluation in Kg
Evaluation of weight loss in Kg from the first appointment and during the different admissions time-points of each patient
Blood pressure measurement
Evaluation of mean blood pressure in mmHg in the first appointment and during the entire trial
Determination of lipid levels
Evaluation of lipid levels in the first appointment and during the entire trial
Determination of renal function
Evaluation of renal function by measuring creatinine levels in the blood in the first appointment and during the entire trial
Assess diabetes quality of life (DQoL) questionnaire
Evaluation of diabetes quality of life (DQoL) questionnaire in the first appointment and during the entire trial. it will measure reliability and validity of a diabetes quality-of-life and will measure the diabetes control and complications. The instrument provides an overall scale score ranging from 0 (lowest DQoL score) to 100 (highest DQoL score), as well as four subscale scores for: 1- satisfaction with treatment, 2- impact of treatment, 3- worry about the future effects of diabetes, and 4- worry about social/vocational issues.
Evaluation of adenosine metabolism in liver and adipose tissue biopsies
evaluation of adenosine receptors protein levels (A1R, A2aR, A2bR) (given in % of protein levels from control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of the 3 receptors levels will allow to evaluate adenosine metabolism in a whole.
Evaluation of adipokines in adipose tissue biopsies
Evaluation of adipokines protein levels (leptin, adiponectin and resistin; given in % of protein levels from control) on adipose tissue collected at the beginning of RYGB surgery. the evaluation of the adipokines levels will allow to evaluate overall adipose tissue function.
Evaluation of cytokines in liver and adipose tissue biopsies
evaluation of cytokines protein levels [interleukin 10 (IL10), tumor necrosis factor alpha (TNFalpha), interleukin 6 (IL6); given in % protein levels from the control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of cytokines on both tissues will allow to determine the overall inflammatory status of the tissues.
Evaluation of inflammatory receptors levels in liver and adipose tissue biopsies
evaluation of inflammatory receptors protein levels (IL10 receptor, TNFalpha receptor, IL6 receptor; given in % protein levels from the control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of cytokines on both tissues will allow to determine the overall inflammatory status of the tissues.

Full Information

First Posted
April 3, 2023
Last Updated
May 15, 2023
Sponsor
Universidade Nova de Lisboa
Collaborators
cruz vermelha hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05859022
Brief Title
Metabolic Effects of Bariatric Arterial Embolization vs Bariatric Surgery
Acronym
BEOD
Official Title
Comparison of Metabolic Effects of Bariatric Arterial Embolization vs. Bariatric Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 16, 2021 (Actual)
Primary Completion Date
October 5, 2023 (Anticipated)
Study Completion Date
June 15, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universidade Nova de Lisboa
Collaborators
cruz vermelha hospital

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
Obesity and Type 2 diabetes mellitus (DMT2) are two of the most common chronic diseases of the Western society. Obesity is one critical factor in DMT2 development, with weight loss having profound beneficial effects on DMT2 and improving the metabolic pathophysiology leading to hyperglycemia. Observational studies reported that surgical intervention of morbid obesity achieved significant improvement of resolution of DMT2, both in short and long-term. Bariatric surgery has been considered the best option for treatment of diabetic obese patients, with the laparoscopic Roux-en-Y Gastric Bypass being the gold standard of the surgical treatment. Bariatric arterial embolization (BAE) technique has proved to be safe effective for weight loss in obese patients, but its metabolic effects have not been studied yet. The hypothesis of the study is that BAE is effective for the resolution of DMT2 inpatients with BMI between 30-43 Kg/m2. The aim is to assess DMT2 remission after BAE and bariatric surgery, to analyze potential conditioning factors, and to compare remission criteria between bariatric surgery and BAE.
Detailed Description
The present project is a prospective, randomized, no-blinded, controlled and interventional clinical single- center study, which seeks to compare the impact of the following interventions: Roux-en-Y gastric By-pass (RYGB) and bariatric arterial embolization (BAE) on metabolic control in patients with DMT2 and BMI between 30-43 Kg/m2 over 2 years. Study initial recruitment will be achieved by an awareness campaign, which will emphasize a study of methods of diabetes management and include identification of patients into treatment at Cruz Vermelha Hospital. The investigator will initially pre-screen patients for the inclusion and exclusion criteria. Detailed information regarding of Diabetes, Obesity and randomization arms of the study would be provided in service meeting. Evaluation of the inclusion and exclusion criteria will occur both at the initial screening visit and the baseline visit prior to randomization. Patients who fail to be include during initial screening may be considered for re-consenting when clinically appropriate, and will have screening/baseline procedures repeated at the discretion of the Investigator. Patients who fail to be include during initial screening based on glycated hemoglobin (HbA1c) and or BMI and are re/screened within 6 months, will only have the baseline HbA1c and BMI repeated. On visit 2 (after 30 days) the 60 patients randomized per study arm for embolization or surgery procedures will be evaluated by the anaesthetist. RYGB or BAE will be scheduled as soon as possible after randomization. After BAE or surgery, patients will be followed 1, 3, 6 and 12 months. At 12 months visit patients will be evaluated for primary endpoint of percent of treatment group achieving HbA1c ≤ 6%. Pre-specified secondary outcomes include measures of glycaemic control, weight loss, mean blood pressure, lipid levels, renal function, assessment of diabetes quality of life (DQoL) and biomarkers in blood. Also, metabolic parameters and other markers will be evaluated from liver and adipose tissue biopsies collected at the beginning of the RYGB surgery to correlate with biochemical evaluations. During the follow-up visits primary and secondary outcomes will be evaluated by different techniques and approaches: body weight loss will be evaluated by bioimpedance analysis; blood will be collected for HbAlc, fasting glucose, lipids, comprehensive Metabolic Panel, Urinalysis (microalbumin and creatinine) and hepatogram by common clinical analysis; the diabetes quality of life (DQoL) question; liver and adipose tissues will be collected during the surgical procedure to asses by western blot the levels of each adenosine receptors, adipokynes, cytokines and inflammatory markers receptors.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Type2diabetes, Bariatric Surgery Candidate, Metabolic Disease
Keywords
bariatric surgery, embolization, intensive medical therapy, BMI, glycemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients assigned for one of 2 arms: Roux-en-Y gastric By-pass (RYGB),bariatric arterial embolization (BAE).
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Roux-en-Y gastric By-pass (RYGB)
Arm Type
Experimental
Arm Description
RYGB procedure requires 1-2 hours of operating time and two to three days length of hospital stay. Use the Kit-RYGB by J& company.
Arm Title
Bariatric Arterial Embolization (BAE)
Arm Type
Experimental
Arm Description
Embosphere Microspheres (EM) are designed to offer controlled, target embolization. BAE procedure requires 1hour of operating time and one day length of hospital stay. Use the Kit by Merit MedicalCompany.
Intervention Type
Other
Intervention Name(s)
Roux-en-Y gastric By-pass (RYGB) surgery
Intervention Description
RYGB procedure requires 1-2 hours of operating time and two to three days length of hospital stay. Use the Kit-RYGB by J& company.
Intervention Type
Other
Intervention Name(s)
Bariatric Arterial Embolization (BAE) procedure
Intervention Description
use of Embosphere Microspheres (EM) that are designed to offer controlled, target embolization.
Primary Outcome Measure Information:
Title
Number of participants with glycated haemoglobin < 6%
Description
The primary outcome of the study will be a level of glycated haemoglobin of 6.0% or less without the use of diabetes medications.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Determination of glycemic level (mg/dL)
Description
Measures of glycemic control by evaluating glycemic level at fast in the blood in mg/dL. less than 126mg/dL will represent a good glycemic control
Time Frame
up to 48 months
Title
Weight evaluation in Kg
Description
Evaluation of weight loss in Kg from the first appointment and during the different admissions time-points of each patient
Time Frame
up to 48 months
Title
Blood pressure measurement
Description
Evaluation of mean blood pressure in mmHg in the first appointment and during the entire trial
Time Frame
up to 48 months
Title
Determination of lipid levels
Description
Evaluation of lipid levels in the first appointment and during the entire trial
Time Frame
up to 48 months
Title
Determination of renal function
Description
Evaluation of renal function by measuring creatinine levels in the blood in the first appointment and during the entire trial
Time Frame
up to 48 months
Title
Assess diabetes quality of life (DQoL) questionnaire
Description
Evaluation of diabetes quality of life (DQoL) questionnaire in the first appointment and during the entire trial. it will measure reliability and validity of a diabetes quality-of-life and will measure the diabetes control and complications. The instrument provides an overall scale score ranging from 0 (lowest DQoL score) to 100 (highest DQoL score), as well as four subscale scores for: 1- satisfaction with treatment, 2- impact of treatment, 3- worry about the future effects of diabetes, and 4- worry about social/vocational issues.
Time Frame
up to 48 months
Title
Evaluation of adenosine metabolism in liver and adipose tissue biopsies
Description
evaluation of adenosine receptors protein levels (A1R, A2aR, A2bR) (given in % of protein levels from control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of the 3 receptors levels will allow to evaluate adenosine metabolism in a whole.
Time Frame
At the beginning of the RYGB surgery
Title
Evaluation of adipokines in adipose tissue biopsies
Description
Evaluation of adipokines protein levels (leptin, adiponectin and resistin; given in % of protein levels from control) on adipose tissue collected at the beginning of RYGB surgery. the evaluation of the adipokines levels will allow to evaluate overall adipose tissue function.
Time Frame
At the beginning of the RYGB surgery
Title
Evaluation of cytokines in liver and adipose tissue biopsies
Description
evaluation of cytokines protein levels [interleukin 10 (IL10), tumor necrosis factor alpha (TNFalpha), interleukin 6 (IL6); given in % protein levels from the control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of cytokines on both tissues will allow to determine the overall inflammatory status of the tissues.
Time Frame
At the beginning of the RYGB surgery
Title
Evaluation of inflammatory receptors levels in liver and adipose tissue biopsies
Description
evaluation of inflammatory receptors protein levels (IL10 receptor, TNFalpha receptor, IL6 receptor; given in % protein levels from the control) on liver and adipose tissue collected at the beginning of RYGB surgery. the evaluation of cytokines on both tissues will allow to determine the overall inflammatory status of the tissues.
Time Frame
At the beginning of the RYGB surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: criteria: Is the candidate for general anesthesia. Body Mass Index (BMI) between 33 and 43 Kg/m2 Patients have a biochemical evidence of Type 2 Diabetes Mellitus (DMT2) confirmed by American Diabetes Association (ADA) criteria: 3.1) treated - HbA1c 7,1%; 3.2) If untreated- fasting 2-hour plasma glucose level of 200 mg/dL during an oral glucose tolerance test and a HbA1c of 7,1%. Willing, able, and mentally competent to provide written informed consent. Able o understand the options and to comply with the requirements of each program. Have a negative urine pregnancy test at screening and baseline visits (prior surgery and Embolization) for women of childbearing potential. Female patients must agree to use reliable method of contraception for 2 years. Exclusion Criteria: Prior bariatric surgery of any kind. Prior complex abdominal surgery including splenectomy, upper GI, anti-reflux surgery and trauma. Abdominal, thoracic, pelvic and/or obstetric-gynaecologic surgery within 3 months or at the discretion of the surgery. Cardiovascular conditions including uncompensated congestive heart failure, dysrhythmia, history of stroke, or uncontrolled hypertension (defined as medically treated with the mean of 3 separate measurements systolic blood pressure (SBP)> 180 mmHg or diastolic blood pressure (DBP) >110mmHg). Patients with coronary artery disease (CAD) that have been successfully treated with coronary artery by-pass graft (CABG) or percutaneous coronary intervention (PCI) or are 1 year after implantation of drug eluting stent and have no evidence of active ischemia are eligible. Known history of chronic liver disease (except for NAFLD/NASH), hepatitis, positive serologic test result for hepatitis B surface antigen and/or hepatitis C antibody, alpha-1-antitrypsin deficiency. Gastrointestinal disorders including a known history of celiac disease and/or other malabsorptive disorders or inflammatory bowel disease (Chron's disease or ulcerative colitis). Psychiatric disorders including dementia, active psychosis, severe depression requiring >2 medications, history of suicide attempts, alcohol or drugs abuse with previous 12months. Pregnancy. Malignancy within 5 years (except squamous cell and basal cell cancer of skin). Anaemia defined as haemoglobin less than 9 in females and 10 in males. Any medical condition requiring anticoagulation therapy that cannot be temporarily discontinued for surgical or embolic approach. Any condition or major illness that, in the investigator's judgment, places the subject at undue risk by participating in the study. Use of investigational therapy or participation in any other clinical trial within 12 weeks prior to signing the informed consent form. Severe pulmonary disease. American Society of Anesthesiologists (ASA) physical status class IV or higher. History of allergy to iodinated contrast media
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rodrigo O. Oliveira, MD
Phone
+351934426720
Email
rtavio.oliveira@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Silvia V. Conde, PhD
Phone
+351918974400
Email
silvia.conde@nms.unl.pt
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodrigo O. Oliveira, MD
Organizational Affiliation
cruz vermelha hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cruz Vermelha Hospital
City
Lisboa
ZIP/Postal Code
1549-008
Country
Portugal
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Otavio O. Oliveira, MD
Phone
+351934426720
Email
rtavio.oliveira@gmail.com
First Name & Middle Initial & Last Name & Degree
Silvia V. Conde, PhD
Phone
+351918974400
Email
silvia.conde@nms.unl.pt
First Name & Middle Initial & Last Name & Degree
Fatima O. Martins, PhD
First Name & Middle Initial & Last Name & Degree
Filipe V. Gomes, MD
First Name & Middle Initial & Last Name & Degree
Tiago Bilhim, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
all individual participant data (IPD) that underlie results in publications and a Philosophy doctor (PhD) thesis
IPD Sharing Time Frame
From 24months some data will be shared and till the end of the project at 48months after recruitment of all patients
IPD Sharing Access Criteria
Results from the present study will be presented in several national and international meetings and published in scientific journals. The PhD dissertation will be done by compiling the articles published in the context of this project.

Learn more about this trial

Metabolic Effects of Bariatric Arterial Embolization vs Bariatric Surgery

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