Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05405205
Other study ID # Slim-LfX2-2021
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date June 8, 2021
Est. completion date August 2022

Study information

Verified date May 2022
Source Slimbiotics GmbH
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this placebo-controlled trial the effect of a synbiotic consisting of three different strains of Lactobacillus fermentum and acacia gum (gum arabic) was compared with a probiotic formulation containing identical strains on body fat mass, body weight management, traits of metabolic syndrome and gut permeability in individuals who are abdominally overweight.


Description:

The effects of probiotics on glucose and lipid metabolism, on body fat, weight, visceral fat and liver steatosis were shown by several meta-analyses for the total variety, as described above. Some probiotic species/strains, however, seem to be more efficacious (Koutnikova et al., 2019). The lactobacilli used in this trial were selected for their anti-inflammatory properties and based on induction of defensins in enterocytes. Therefore, one may expect more pronounced effects of these strains on traits of the metabolic syndrome, which is driven by low grade inflammation, than those found in the meta-analyses for the whole variety of probiotics without discriminating species and strain specificity. The combination of these Lactobacillus strains with acacia gum is expected to enable even more pronounce effects, since acacia gum was shown to increase the number of lactobacilli in the gut (Cherbut et al., 2003; Calame et al., 2008) and, hence, are supposed to promote their propagation and, hence their effects. The dosage of 10 g/day acacia gum was demonstrated to be sufficient for enhancing fecal lactobacilli and bifidobacterial (Cherbut et al., 2003; Calame et al., 2008). Acacia gum, however, seems to have own effects on traits of the metabolic syndrome. Even though the effects still need to be confirmed in more DB-RCTs, one may suggest a separate effect, e.g. by reduction of the SGLT1in the intestine (Nasir et al., 2010). This DB-RCT aims at providing first evidence for an effect of this symbiotic on traits of the metabolic syndrome. The target parameters were selected for allowing a health claim according to the Health Claim Directive of the EU (REGULATION (EC) No 1924/2006 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 20 December 2006 on Nutrition and Health Claims Made on Foods) and/or the REGULATION (EU) No 609/2013 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 12 June 2013 for Food for Special Medical Purposes after having confirmative evidence. The following health claim options are feasible according to the EFSA Guidance on the scientific requirements for health claims related to appetite ratings, weight management, and blood glucose concentrations (EFSA Journal 2012;10(3):2604) and to the EFSA Guidance on the scientific requirements for health claims related to antioxidants, oxidative damage and cardiovascular health (EFSA Journal 2011;9(12):2474): - Beneficial effect on long-term glycemia (glucose metabolism) as assessed by HbA1c, - facilitates weight management as assessed by body weight, BMI, waist circumference, or body fat mass, - reduces insulin resistance, a risk factor for type 2 diabetes, as assessed by HOMA-IR, - reduces LDL-C, a risk factor coronary heart disease, - increases HDL-C, a beneficial physiological effect. It is noteworthy that EFSA admits demonstration of effects in type 2 diabetes for health claims on these target parameters assuming that there is a continuity of these parameters from healthy to impaired metabolism (EFSA Journal 2012;10(3):2604). Alternatively, the following claims may be used as FSMPs: - For dietary management of impaired glucose metabolism and type 2 diabetes - for dietary weight management in overweight - for dietary management of insulin resistance The primary parameter has been selected by estimating the sample size for these potential targets based on the most recent meta-analysis of Koutnikova et al. 2019. Since we expect a more pronounced effect by the selected strains and the combination with acacia gum (see above) we assumed a twofold higher effect than found for the whole variety of probiotics. Taking this into account, the target parameter with the lowest estimated sample size was body fat in individuals with type 2 diabetes (N = 56 for each arm). Accordingly, this target was defined as primary parameter.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 180
Est. completion date August 2022
Est. primary completion date June 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Overweight or obese (BMI = 25) - Elevated waist circumference (>94cm and >80cm (for European men and women, respectively) - Age = 18 - Written informed consent Exclusion Criteria: - Subjects currently enrolled in another clinical study - Subjects having finished another clinical study within the last 4 weeks before inclusion - Hypersensitivity, allergy or intolerance against any compound of the test products (e. g. acacia gum) - Condition after implantation of a cardiac pacemaker or other active implants - Sulfonylurea treatment - Any disease or condition which might compromise significantly the hepatic (ascites), hematopoietic, renal, endocrine, pulmonary, central nervous, cardiovascular, immunological, dermatological, gastrointestinal or any other body system with the exception of the conditions defined by the inclusion criteria - History of or present liver deficiency as defined by Quick < 70% - Regular medical treatment including OTC, which may have impact on the study aims (e. g. probiotics containing supplements, laxatives, steroids etc.) - History of hepatitis B, C, HIV - Major cognitive or psychiatric disorders - Subjects who are scheduled to undergo any diagnostic intervention or hospitalization which may cause protocol deviations - Simultaneous study participation by members of the same household - Pregnancy and lactation - Ascites as assessed by sonography - Any diet to lose body weight - Eating disorders or vegan diet - Anorexic drugs - Present drug abuse or alcoholism - Legal incapacity

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
synbiotic
Consumption of 6 g powder consisting of the strains Lactobacillus fermentum K7-Lb1, L. fermentum K8- Lb1, L. fermentum K11-Lb3, acacia gum (gum arabic), maltodextrin, sucralose and flavour twice a day resolved in drinking water
probiotic
Consumption of 6 g powder consisting of the strains Lactobacillus fermentum K7-Lb1, L. fermentum K8- Lb1, L. fermentum K11-Lb3, maltodextrin, sucralose and flavour twice a day resolved in drinking water
placebo
Consumption of 6 g powder containing microcrystalline cellulose, maltodextrin , sucralose and flavour twice a day, resolved in drinking water

Locations

Country Name City State
Germany Clincal Research Center Kiel GmbH Kiel Schleswig-Holstein

Sponsors (2)

Lead Sponsor Collaborator
Slimbiotics GmbH Clinical Research Center Kiel GmbH

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Other HOMA-IR HOMA-IR (Homeostasis Model Assessment (HOMA)-IR = glucose [mmol/L] x insulin [µU/ml]/22,5) as parameter for insulin resistance 12 weeks
Other MSX-index MSX-index (alteration V3-V1) according to ATP III/IDF* definitions (Waist x FPG x Tg x 1/HDL-C x BPsys x BPdias) (ascites as interfering cause for alteration of these measures will be excluded by abdominal sonography) 12 weeks
Other Sagittal abdominal diameter (SAD) Sagittal abdominal diameter (SAD): Distance between the under surface of the rectus muscle and the anterior wall of the aorta - measure for visceral fat after Armellini et al. 1991: Sagittal abdominal diameter as a practical predictor of visceral fat, Int J Obes. 1991 12 weeks
Primary Body Fat Mass Body Fat Mass (BFM) as assessed by bioelectrical impedance analysis (BIA) (alteration V3-V1; synbiotic versus placebo 12 weeks
Secondary Visceral Adiposity Index Visceral Adiposity Index (VAI) after Amato et al. Diabetes Care 33:920-922, 2010: (Females: VAI = WC / (36.58 + (1.89 × BMI)) × (TG/0.81) × (1.52/HDL)), (Males: VAI = (WC / (39.68 + (1.88 × BMI)) × (TG/1.03) × (1.31/HDL) 12 weeks
See also
  Status Clinical Trial Phase
Recruiting NCT05942326 - Sleep Goal-focused Online Access to Lifestyle Support N/A
Completed NCT04587752 - Cognitive-Behavioral Therapy for Weight-related Bullying (Online Treatment) N/A
Completed NCT03506074 - Flavor Test Results in General Population
Completed NCT04153578 - Time to Lose the Weight? Comparison of Weight-based and Non-weight-based Vasopressors for Septic Shock
Completed NCT03712098 - Daily Liraglutide for Nicotine Dependence Phase 2
Active, not recruiting NCT04537988 - eCHANGE: eHealth Design to Facilitate Weight Maintenance Following Initial Weight Loss N/A
Recruiting NCT05826184 - Time Restricted Eating With or Without a Fiber Supplement for Weight Management in Pediatric Cancer Survivors N/A
Completed NCT05900843 - Weight Abnormalities With Diet and Exercise Frequency in Egyptian Children With Cerebral Palsy
Active, not recruiting NCT05107609 - Psychobiological Processes in Social Evaluation N/A
Completed NCT03597061 - Healthy Start to Feeding Intervention N/A
Not yet recruiting NCT06299644 - Endoscopic Sleeve Gastroplasty Technique Comparison for Weight Loss N/A
Completed NCT04063059 - Black Women's Wellness Project N/A
Recruiting NCT05775016 - Effects of Adding L-BAIBA to Exercising Adult Overweight and Obese Men and Women N/A
Not yet recruiting NCT04898439 - GReen And Healthy Schools N/A
Completed NCT03867279 - Flossing Technique With Neuromuscular Reeducation Exercises in Trained Subjects N/A
Completed NCT04780828 - Investigation of the Effects of Different Levels of Obesity on the Respiratory System
Not yet recruiting NCT06281938 - Machine Learning and 3D Image-based Modeling for Body Weight Estimation. N/A
Completed NCT05456594 - Comparing Sports Bra Design in Full Busted Women N/A
Completed NCT03342430 - Early Dieting in Girls: a Longitudinal Cohort Study N/A
Not yet recruiting NCT05878444 - Evaluation of the Colonization Capacity of a Probiotic Bacterium. Phase 1