Bariatric Endoscopy and NAFLD
Primary Purpose
Obesity, NAFLD, Liver Steatosis
Status
Recruiting
Phase
Not Applicable
Locations
Czechia
Study Type
Interventional
Intervention
bariatric endoscopy, mainly intragastric baloons, plication of stomach too
Sponsored by
About this trial
This is an interventional treatment trial for Obesity focused on measuring Obesity, NAFLD, liver steatosis, liver fibrosis, bariatric endoscopy, weight lose
Eligibility Criteria
Inclusion Criteria:
To be eligible for participation in this study, subjects must conform to the following inclusion criteria:
- Age between 21-64 years;
- BMI >30 Kg/m2
- Must be able to comply with all study requirements for the duration of the study as outlined in the protocol. This includes complying with the visit schedule as well as study specific procedures such as: clinical assessment , endoscopy, radiography, as well as laboratory investigations.
- Must be able to understand and be willing to provide written informed consent.
Exclusion Criteria:
Subjects meeting any of the following exclusionary criteria cannot be enrolled in the study:
- Achalasia and any other esophageal motility disorders
- Heart diseases: unstable angina, myocardial infarction within the past year, or heart disease classified within the New York Heart Association's Class III or IV functional capacity.
- Hypertension: uncontrolled hypertension during last 3 month
- Severe renal, hepatic, pulmonary disease or cancer;
- GIT stenosis or obstruction
- Pregnancy or breastfeeding
- Impending gastric surgery 60 days post intervention;
- Currently participating in other study
- Celiac disease
- History of bariatric surgery
- Chronic or recent acute pancreatitis
- Type 2 diabetes with insuline medication or type 1 diabetes
- Hematologic disease or disease with impairment of hemocoagulation
- Decompensated psychiatric disease
- Autoimmune disease with chronic glucocorticoid or imunosupressive medications
- Uncontroled disease of thyroid gland
- Excesive abuse of addictive substances such alcohol or other
Sites / Locations
- Department of gastroenterology, hepatology and pancreatologyRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Group with adjustable IGB
Group with nin-adjustable IGB
Arm Description
Outcomes
Primary Outcome Measures
Amount of patients with NAFLD with degree of fibrosis of the liver amog patients undergoing bariatric endoscopy and determine influence of bariatric endoscopy on clinical course of NAFLD and liver fibrosis
Amount of patients with NAFLD with degree of fibrosis of the liver amog patients undergoing bariatric endoscopy and determine influence of bariatric endoscopy on clinical course of NAFLD and liver fibrosis
Secondary Outcome Measures
Influence of bariatric endoscopy on improvements of weight, antropometric, improvements in components of metabolic syndrome
Influence of bariatric endoscopy on improvements of weight, antropometric, improvements in components of metabolic syndrome
Full Information
NCT ID
NCT04669470
First Posted
December 9, 2020
Last Updated
December 9, 2020
Sponsor
University of Ostrava
Collaborators
University Hospital Olomouc, University Hospital Ostrava, Palacky University
1. Study Identification
Unique Protocol Identification Number
NCT04669470
Brief Title
Bariatric Endoscopy and NAFLD
Official Title
Influence of Bariatric Endoscopy on Clinical Course of NAFLD
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2020 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Ostrava
Collaborators
University Hospital Olomouc, University Hospital Ostrava, Palacky University
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
Find out how bariatric endocopy will influence clinical course of non alcoholic fatty liver disease.
Detailed Description
The study will test and investigate the impact of bariatric endoscopy (various types of intragastric balloons, endoscopic sleeve gastroplasty, aspiration therapy) on components of the metabolic syndrome in obese patients, especially on influencing non-alcoholic steatosis and steatohepatitis and signs of liver fibrotization and weight reduction. The method consists in performing a mini-invasive endoscopic procedure and, as a result, in reduced food intake.
Current state of knowledge:
Based on data evaluated according to EBM (Evidence Based Medicine), it is an indisputable fact that bariatric methods have a demonstrable effect not only on improving the parameters and regression of many metabolic syndromes, but also improve the course of non-alcoholic fatty liver disease (NAFLD). It is this nosological unit that is becoming the dominant cause of liver disease in developed countries and has two subunits, where simple hepatic steatosis (NAFL) is considered a benign disease, while the second, where fat accumulation in the liver is associated with the inflammatory process called non-alcoholic steatohepatitis (NASH). ) has serious consequences for the liver with the development of fibrotization leading to cirrhosis with all its adverse effects. Recently, however, it has been shown that even simple steatosis is not as benign as it seemed, but carries an independent risk for the patient due to an increased incidence of cardiovascular diseases, oncological manifestations and a higher incidence of metabolic syndrome manifestations. Classical bariatric endoscopy carries a number of risks associated with the patient for the surgical procedure, however, we also have less invasive methods of gradually more and more developing endoscopy and dreams of associated bariatric procedures with many times lower risk for the patient.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, NAFLD, Liver Steatosis, Liver Fibrosis
Keywords
Obesity, NAFLD, liver steatosis, liver fibrosis, bariatric endoscopy, weight lose
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group with adjustable IGB
Arm Type
Active Comparator
Arm Title
Group with nin-adjustable IGB
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
bariatric endoscopy, mainly intragastric baloons, plication of stomach too
Intervention Description
bariatric endoscopy, mainly intragastric baloons, plication of stomach too
Primary Outcome Measure Information:
Title
Amount of patients with NAFLD with degree of fibrosis of the liver amog patients undergoing bariatric endoscopy and determine influence of bariatric endoscopy on clinical course of NAFLD and liver fibrosis
Description
Amount of patients with NAFLD with degree of fibrosis of the liver amog patients undergoing bariatric endoscopy and determine influence of bariatric endoscopy on clinical course of NAFLD and liver fibrosis
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Influence of bariatric endoscopy on improvements of weight, antropometric, improvements in components of metabolic syndrome
Description
Influence of bariatric endoscopy on improvements of weight, antropometric, improvements in components of metabolic syndrome
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
To be eligible for participation in this study, subjects must conform to the following inclusion criteria:
Age between 21-64 years;
BMI >30 Kg/m2
Must be able to comply with all study requirements for the duration of the study as outlined in the protocol. This includes complying with the visit schedule as well as study specific procedures such as: clinical assessment , endoscopy, radiography, as well as laboratory investigations.
Must be able to understand and be willing to provide written informed consent.
Exclusion Criteria:
Subjects meeting any of the following exclusionary criteria cannot be enrolled in the study:
Achalasia and any other esophageal motility disorders
Heart diseases: unstable angina, myocardial infarction within the past year, or heart disease classified within the New York Heart Association's Class III or IV functional capacity.
Hypertension: uncontrolled hypertension during last 3 month
Severe renal, hepatic, pulmonary disease or cancer;
GIT stenosis or obstruction
Pregnancy or breastfeeding
Impending gastric surgery 60 days post intervention;
Currently participating in other study
Celiac disease
History of bariatric surgery
Chronic or recent acute pancreatitis
Type 2 diabetes with insuline medication or type 1 diabetes
Hematologic disease or disease with impairment of hemocoagulation
Decompensated psychiatric disease
Autoimmune disease with chronic glucocorticoid or imunosupressive medications
Uncontroled disease of thyroid gland
Excesive abuse of addictive substances such alcohol or other
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Adam Vasura
Phone
420597374191
Email
obezita@fno.cz
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adam Vasura, MD
Organizational Affiliation
- Department of gastroenterology, hepatology and pancreatology, Internal clinic, University hospital Ostrava
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Evzen Machytka
Organizational Affiliation
Department of gastroenterology, hepatology and pancreatology, Internal clinic, University hospital Ostrava
Official's Role
Study Chair
Facility Information:
Facility Name
Department of gastroenterology, hepatology and pancreatology
City
Ostrava
ZIP/Postal Code
70800
Country
Czechia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adam Vasura
Phone
+420597374191
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
30683512
Citation
Fakhry TK, Mhaskar R, Schwitalla T, Muradova E, Gonzalvo JP, Murr MM. Bariatric surgery improves nonalcoholic fatty liver disease: a contemporary systematic review and meta-analysis. Surg Obes Relat Dis. 2019 Mar;15(3):502-511. doi: 10.1016/j.soard.2018.12.002. Epub 2018 Dec 6.
Results Reference
background
PubMed Identifier
21553304
Citation
Machytka E, Klvana P, Kornbluth A, Peikin S, Mathus-Vliegen LE, Gostout C, Lopez-Nava G, Shikora S, Brooks J. Adjustable intragastric balloons: a 12-month pilot trial in endoscopic weight loss management. Obes Surg. 2011 Oct;21(10):1499-507. doi: 10.1007/s11695-011-0424-z.
Results Reference
background
PubMed Identifier
30122876
Citation
Leoni S, Tovoli F, Napoli L, Serio I, Ferri S, Bolondi L. Current guidelines for the management of non-alcoholic fatty liver disease: A systematic review with comparative analysis. World J Gastroenterol. 2018 Aug 14;24(30):3361-3373. doi: 10.3748/wjg.v24.i30.3361.
Results Reference
background
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Bariatric Endoscopy and NAFLD
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