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Impact of a Specific Micronutrient-probiotic-supplement on Fatty Liver of Patients After Mini-Gastric Bypass Surgery (FMG-01)

Primary Purpose

Obesity, Gastric Bypass, NAFLD

Status
Completed
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Micronutrient-probiotic-combination
Micronutrient-placebo-combination
Sponsored by
Bonn Education Association for Dietetics r.A., Cologne, Germany
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Bariatric surgery, Obesity, NAFLD, Micronutrient supplementation, Probiotic supplementation

Eligibility Criteria

20 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • subjects 20-65 years old
  • BMI ≥ 35 kg/m² to ≤ 50 kg/m²
  • Fatty Liver Index ≥ 60

Exclusion Criteria:

  • subjects with anamnestic known alcoholic-fatty liver disease, hepatitis B, hepatitis C, HIV/ AIDS
  • subjects with chronic conditions such as active malignant disease, inflammatory bowel disease and other systemic inflammatory conditions
  • supplementation with dietary supplements or drugs which contain probiotics, milk thistle, fatty acids, vitamins or minerals 4 weeks before bariatric surgery
  • treatment with psychotropic drugs
  • diabetic patients who are treated with antidiabetic medications
  • use of antibiotic 4 weeks before bariatric surgery
  • weight gain during run-in phase of more than 5 %
  • in women of childbearing age, pregnancy or breastfeeding
  • no safe method of contraception in women of childbearing age

Sites / Locations

  • St. Franziskus-Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Specific Micronutrient-probiotic-combination

Micronutrient-placebo-combination

Arm Description

Intake of one micronutrient capsule three times daily and probiotic powder twice daily starting on the first day after hospital discharge until 12 weeks postoperatively. The micronutrient capsules consist of vitamins, minerals, phytochemicals and bioactive substances. The probiotic supplement is a powder of 10 different species of probiotic bacteria.

Intake of one micronutrient capsule three times daily and placebo powder twice daily starting on the first day after hospital discharge until 12 weeks postoperatively. The micronutrient-control-combination consists of a micronutrient capsule (vitamins and minerals) but without phytochemicals and bioactive substances, and a placebo powder manufactured to mimic the probiotic powder.

Outcomes

Primary Outcome Measures

Change in alanine-aminotransferase (ALAT) activity in serum
ALAT in U/l

Secondary Outcome Measures

Change in Fatty Liver Index (FLI)
FLI will be calculated as: [e 0.953 x loge (triglycerides (mg/dl)) + 0.139 x BMI (kg/m²) + 0.718 x loge (GGT (U/l)) + 0.053 x waist circumference (cm) - 15.745) / (1 + e 0.953 x loge (triglycerides (mg/dl)) + 0.139 x BMI (kg/m²) + 0.718 x loge (GGT (U/l)) + 0.053 x waist circumference (cm) - 15.745)] × 100. A FLI < 30 rules out fatty liver and a FLI > 60 rules in fatty liver.
Change in nonalcoholic fatty liver disease (NAFLD) Fibrosis Score (NFS)
NFS will be calculated as: - 1.675 + 0.037 x age (years) + 0.094 x BMI (kg/m²) + 1.13 x impaired fasting glucose (IFG)/diabetes (yes = 1, no = 0) + 0.99 x aspartate aminotransferase (ASAT)/ALAT ratio - 0.013 x platelet (x10^9) - 0.66 x albumin (g/dl). NFS > 0.676 is considered to be diagnostic for the presence of significant fibrosis. NFS < -1.455 is considered to be diagnostic fot the absence if fibrosis. NFS scores between -1.455 and 0.675 are referred as "indeterminate" scores.
Change in fasting glucose concentration
Fasting glucose in mmol/l
Change in fasting insulin concentration
Fasting insulin in pmol/l
Change in homeostatic model assessment (HOMA) of insulin resistance (IR) (HOMA-IR)
HOMA-IR will be calculated as: fasting insulin (μU/ml) x fasting glucose (mmol/l) / 22.5. HOMA-IR > 2.77 is considered to be diagnostic for insulin resistance.
Change in glycated haemoglobin (HbA1c)
Intervention change in HbA1c level
Change in resting blood pressure
Intervention changes in resting blood pressure in mmHg
Change in heart rate
Intervention changes in heart rate in bpm

Full Information

First Posted
June 7, 2018
Last Updated
September 23, 2020
Sponsor
Bonn Education Association for Dietetics r.A., Cologne, Germany
Collaborators
St. Franziskus Hospital, University of Bonn, FormMed HealthCare AG
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1. Study Identification

Unique Protocol Identification Number
NCT03585413
Brief Title
Impact of a Specific Micronutrient-probiotic-supplement on Fatty Liver of Patients After Mini-Gastric Bypass Surgery
Acronym
FMG-01
Official Title
Impact of a Specific Micronutrient-probiotic-combination on Fatty Liver and Cardiometabolic Status of Obese Patients After Mini-Gastric Bypass Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
August 31, 2018 (Actual)
Primary Completion Date
January 17, 2020 (Actual)
Study Completion Date
January 17, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bonn Education Association for Dietetics r.A., Cologne, Germany
Collaborators
St. Franziskus Hospital, University of Bonn, FormMed HealthCare AG

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
Aim of this prospective randomized intervention study is to evaluate the effect of a dietary intervention with a specific micronutrient-probiotic-combination for 12 weeks on fatty liver and cardiometabolic status in obese, nonalcoholic fatty liver disease (NAFLD) patients after Mini-Gastric Bypass (MGB) surgery.
Detailed Description
Background: The increasing prevalence of obesity and diabetes mellitus seems to reach epidemic proportions worldwide. In particular visceral obesity in combination with impaired glucose tolerance is associated with risk for progression of a broad spectrum of cardiometabolic diseases such as type 2 diabetes, hypertension, dyslipidemia, cardiovascular disease and non-alcoholic fatty liver disease (NAFLD). Thus, among patients undergoing bariatric surgery more than 95% have NAFLD, with nonalcoholic steatohepatitis (NASH) being present in 32-39 %. Only bariatric surgery currently seems to attain long-term weight loss in morbidly obese patients. In addition, greater success in terms of improvement in obesity related comorbidities and reduction of overall-mortality can be achieved by surgical measures. Recent data indicate that Mini-Gastric Bypass (MGB) is an effective procedure for weight loss and reduction of comorbidities. Although weight loss is usually recommended as therapy for obesity with NAFLD and NASH, not all NAFLD patients benefit from surgical induced weight loss as indicated by increase in transaminase activity. An optimized micronutrient in combination with a probiotic supplementation could be a useful tool to prevent the transition from NAFLD to NASH. Aim: Therefore this study aims to elucidate the effect of a specific micronutrient-probiotic-combination on fatty liver and insulin resistance in obese patients after MGB surgery. Furthermore, this study aims to help optimizing the dietary food supplementation after MGB to reduce the progress of NAFLD/NASH and cardiometabolic diseases. Methods: A randomized double blind clinical trial of 12 week dietary intervention with a specific micronutrient-probiotic-combination will be conducted in obese patients with NAFLD after standardized MGB surgery. To this end, a total of 60 patients will be randomly assigned to a specific micronutrient-probiotic-combination or micronutrient-placebo-combination group. During the preoperative 4-week run-in phase, each patient receives a formula diet to improve protein and micronutrient supply. This should align the metabolic situation within the study group. At baseline and study end blood samples are taken for further analysis of metabolic, clinical and biochemical parameters. Anthropometric data (body height, body weight, and waist circumference) and bioelectrical impedance analysis are also collected at the beginning and after 8 and 12 weeks. Fecal samples will be collected prior to surgery and after 4, 8 and 12 weeks (concomitant variable). All patients will fill out validated food intake questionnaires and stool questionnaires (frequency and consistence) after 4, 8 and 12 weeks (concomitant variable).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Gastric Bypass, NAFLD
Keywords
Bariatric surgery, Obesity, NAFLD, Micronutrient supplementation, Probiotic supplementation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
prospective, randomized, placebo-controlled, double-blind interventional study
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Specific Micronutrient-probiotic-combination
Arm Type
Active Comparator
Arm Description
Intake of one micronutrient capsule three times daily and probiotic powder twice daily starting on the first day after hospital discharge until 12 weeks postoperatively. The micronutrient capsules consist of vitamins, minerals, phytochemicals and bioactive substances. The probiotic supplement is a powder of 10 different species of probiotic bacteria.
Arm Title
Micronutrient-placebo-combination
Arm Type
Placebo Comparator
Arm Description
Intake of one micronutrient capsule three times daily and placebo powder twice daily starting on the first day after hospital discharge until 12 weeks postoperatively. The micronutrient-control-combination consists of a micronutrient capsule (vitamins and minerals) but without phytochemicals and bioactive substances, and a placebo powder manufactured to mimic the probiotic powder.
Intervention Type
Dietary Supplement
Intervention Name(s)
Micronutrient-probiotic-combination
Intervention Description
Specific combined micronutrient-probiotic-supplement with different vitamins, minerals, phytochemicals and bioactive substances, and a mixture of 10 different probiotic bacteria.
Intervention Type
Dietary Supplement
Intervention Name(s)
Micronutrient-placebo-combination
Intervention Description
micronutrient (capsule)-placebo (powder)-supplement
Primary Outcome Measure Information:
Title
Change in alanine-aminotransferase (ALAT) activity in serum
Description
ALAT in U/l
Time Frame
Baseline and 12 weeks
Secondary Outcome Measure Information:
Title
Change in Fatty Liver Index (FLI)
Description
FLI will be calculated as: [e 0.953 x loge (triglycerides (mg/dl)) + 0.139 x BMI (kg/m²) + 0.718 x loge (GGT (U/l)) + 0.053 x waist circumference (cm) - 15.745) / (1 + e 0.953 x loge (triglycerides (mg/dl)) + 0.139 x BMI (kg/m²) + 0.718 x loge (GGT (U/l)) + 0.053 x waist circumference (cm) - 15.745)] × 100. A FLI < 30 rules out fatty liver and a FLI > 60 rules in fatty liver.
Time Frame
Baseline and 12 weeks
Title
Change in nonalcoholic fatty liver disease (NAFLD) Fibrosis Score (NFS)
Description
NFS will be calculated as: - 1.675 + 0.037 x age (years) + 0.094 x BMI (kg/m²) + 1.13 x impaired fasting glucose (IFG)/diabetes (yes = 1, no = 0) + 0.99 x aspartate aminotransferase (ASAT)/ALAT ratio - 0.013 x platelet (x10^9) - 0.66 x albumin (g/dl). NFS > 0.676 is considered to be diagnostic for the presence of significant fibrosis. NFS < -1.455 is considered to be diagnostic fot the absence if fibrosis. NFS scores between -1.455 and 0.675 are referred as "indeterminate" scores.
Time Frame
Baseline and 12 weeks
Title
Change in fasting glucose concentration
Description
Fasting glucose in mmol/l
Time Frame
Baseline and 12 weeks
Title
Change in fasting insulin concentration
Description
Fasting insulin in pmol/l
Time Frame
Baseline and 12 weeks
Title
Change in homeostatic model assessment (HOMA) of insulin resistance (IR) (HOMA-IR)
Description
HOMA-IR will be calculated as: fasting insulin (μU/ml) x fasting glucose (mmol/l) / 22.5. HOMA-IR > 2.77 is considered to be diagnostic for insulin resistance.
Time Frame
Baseline and 12 weeks
Title
Change in glycated haemoglobin (HbA1c)
Description
Intervention change in HbA1c level
Time Frame
Baseline and 12 weeks
Title
Change in resting blood pressure
Description
Intervention changes in resting blood pressure in mmHg
Time Frame
Baseline and 12 weeks
Title
Change in heart rate
Description
Intervention changes in heart rate in bpm
Time Frame
Baseline and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: subjects 20-65 years old BMI ≥ 35 kg/m² to ≤ 50 kg/m² Fatty Liver Index ≥ 60 Exclusion Criteria: subjects with anamnestic known alcoholic-fatty liver disease, hepatitis B, hepatitis C, HIV/ AIDS subjects with chronic conditions such as active malignant disease, inflammatory bowel disease and other systemic inflammatory conditions supplementation with dietary supplements or drugs which contain probiotics, milk thistle, fatty acids, vitamins or minerals 4 weeks before bariatric surgery treatment with psychotropic drugs diabetic patients who are treated with antidiabetic medications use of antibiotic 4 weeks before bariatric surgery weight gain during run-in phase of more than 5 % in women of childbearing age, pregnancy or breastfeeding no safe method of contraception in women of childbearing age
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karl Peter Rheinwalt, MD
Organizational Affiliation
St. Franziskus Hospital, Cologne and Bonn Education Association for Dietetics r.A., Cologne, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Franziskus-Hospital
City
Cologne
ZIP/Postal Code
50825
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34919684
Citation
Crommen S, Rheinwalt KP, Plamper A, Simon MC, Rosler D, Fimmers R, Egert S, Metzner C. A Specifically Tailored Multistrain Probiotic and Micronutrient Mixture Affects Nonalcoholic Fatty Liver Disease-Related Markers in Patients with Obesity after Mini Gastric Bypass Surgery. J Nutr. 2022 Feb 8;152(2):408-418. doi: 10.1093/jn/nxab392.
Results Reference
derived

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Impact of a Specific Micronutrient-probiotic-supplement on Fatty Liver of Patients After Mini-Gastric Bypass Surgery

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