Clinical Trials Directory

Trials / Completed

CompletedNCT03548480

Targeting the Gut Microbiome for Prader-Willi Syndrome Treatment

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Fundació Sant Joan de Déu · Academic / Other
Sex
All
Age
2 Years – 19 Years
Healthy volunteers
Not accepted

Summary

The gut microbiome has recently emerged as a major contributor to obesity, systemic inflammation, and metabolic disease. Furthermore, intestinal bacteria are crucial players in the gut-brain axis, regulating a broad range of central nervous system processes, from satiety mechanisms to anxiety and social behavior. Thus, targeting the microbiome is being actively investigated as a therapeutic strategy for a wide array of diseases, including obesity, anxiety, depression, and autism. Among all intestinal bacteria, Bifidobacterium animalis spp. lactis (BAL) has shown promise for obesity treatment in experimental animal models and human subjects, improving body composition and metabolic health, and reducing energy intake. Moreover, tryptophan metabolism, a crucial regulator of satiety mechanisms and anxiety, is a main target of BAL. Given that clinical manifestations of Prader-Willi syndrome (PWS) include hyperphagia, anxiety, altered body composition, and metabolic dysregulation, the aforementioned effects of BAL might prove highly beneficial for children with PWS. Here, the investigators will test this hypothesis by performing a randomized double-blinded placebo-controlled crossover clinical study to assess the effects of BAL supplementation on an array of clinical manifestations of PWS. Children with PWS will undergo a 3-month placebo/probiotic treatment period, a 3-month washout period, followed by a 3-month probiotic/placebo supplementation. Anthropometric, biochemical, and psychological data as well as biological samples will be obtained at the beginning of the study, and after each of the study periods, with a total of four time-points. Specifically, the investigators will determine body composition by DXA analysis; metabolic health by assessing glucose and lipid metabolic parameters as well as circulating hormonal and cytokine levels; thermoregulation by non-invasive thermal imaging; and hyperphagia and emotional and behavioral problems by applying parental-rated validated questionnaires.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPlaceboIntervention with a daily dose of placebo
DIETARY_SUPPLEMENTProbioticIntervention with a daily dose of probiotic

Timeline

Start date
2018-01-01
Primary completion
2019-01-31
Completion
2019-01-31
First posted
2018-06-07
Last updated
2020-03-05

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT03548480. Inclusion in this directory is not an endorsement.