Metabolic Effects of Bariatric Arterial Embolization vs Bariatric Surgery

Obesity Clinical Trial

— BEOD  

Official title:

Comparison of Metabolic Effects of Bariatric Arterial Embolization vs. Bariatric Surgery

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05859022
• Other study ID #: BEOD trial
• Status: Recruiting
• Phase: N/A
• Start date: June 16, 2021
• Est. completion date: October 2025

Study information

• Verified date: May 2024
• Source: Universidade Nova de Lisboa
• Contact: Rodrigo O. Oliveira, MD
• Phone: +351934426720
• Email: rtavio.oliveira[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: October 2025
• Est. primary completion date: August 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• criteria:

1. Is the candidate for general anesthesia.

2. Body Mass Index (BMI) between 33 and 43 Kg/m2

3. 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%.

4. Willing, able, and mentally competent to provide written informed consent.

5. Able o understand the options and to comply with the requirements of each program.

6. Have a negative urine pregnancy test at screening and baseline visits (prior surgery and Embolization) for women of childbearing potential.

7. Female patients must agree to use reliable method of contraception for 2 years.

Exclusion Criteria:

1. Prior bariatric surgery of any kind.

2. Prior complex abdominal surgery including splenectomy, upper GI, anti-reflux surgery and trauma.

3. Abdominal, thoracic, pelvic and/or obstetric-gynaecologic surgery within 3 months or at the discretion of the surgery.

4. 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.

5. 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.

6. Gastrointestinal disorders including a known history of celiac disease and/or other malabsorptive disorders or inflammatory bowel disease (Chron's disease or ulcerative colitis).

7. Psychiatric disorders including dementia, active psychosis, severe depression requiring >2 medications, history of suicide attempts, alcohol or drugs abuse with previous 12months.

8. Pregnancy.

9. Malignancy within 5 years (except squamous cell and basal cell cancer of skin).

10. Anaemia defined as haemoglobin less than 9 in females and 10 in males.

11. Any medical condition requiring anticoagulation therapy that cannot be temporarily discontinued for surgical or embolic approach.

12. Any condition or major illness that, in the investigator's judgment, places the subject at undue risk by participating in the study.

13. Use of investigational therapy or participation in any other clinical trial within 12 weeks prior to signing the informed consent form.

14. Severe pulmonary disease.

15. American Society of Anesthesiologists (ASA) physical status class IV or higher.

16. History of allergy to iodinated contrast media

Related Conditions & MeSH terms

• Bariatric Surgery Candidate
• Metabolic Disease
• Metabolic Diseases
• Obesity

Intervention

Other:
• Roux-en-Y gastric By-pass (RYGB) surgery
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.
• Bariatric Arterial Embolization (BAE) procedure
use of Embosphere Microspheres (EM) that are designed to offer controlled, target embolization.

Locations

Country	Name	City	State
Portugal	Cruz Vermelha Hospital	Lisboa

Sponsors (2)

Lead Sponsor	Collaborator
Universidade Nova de Lisboa	cruz vermelha hospital

Country where clinical trial is conducted

Portugal, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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.	12 months
Secondary	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	up to 48 months
Secondary	Weight evaluation in Kg	Evaluation of weight loss in Kg from the first appointment and during the different admissions time-points of each patient	up to 48 months
Secondary	Blood pressure measurement	Evaluation of mean blood pressure in mmHg in the first appointment and during the entire trial	up to 48 months
Secondary	Determination of lipid levels	Evaluation of lipid levels in the first appointment and during the entire trial	up to 48 months
Secondary	Determination of renal function	Evaluation of renal function by measuring creatinine levels in the blood in the first appointment and during the entire trial	up to 48 months
Secondary	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.	up to 48 months
Secondary	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.	At the beginning of the RYGB surgery
Secondary	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.	At the beginning of the RYGB surgery
Secondary	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.	At the beginning of the RYGB surgery
Secondary	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.	At the beginning of the RYGB surgery