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Recruiting NCT07529119

Effect of Consuming a Mango and Chia-based Beverage on Modulating the Intestinal Microbiota in Obese Children

No phase Interventional Microbiota

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Mango juice, Mango and chia juice.
Who it may be relevant to
Registry conditions: Microbiota. Basic parameters: 8 years — 16 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Paraguay
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This randomized clinical trial evaluates the effect of a mango and chia-based beverage on gut microbiota modulation in 100 Paraguayan children aged 8-16 years with obesity. Participants will consume the intervention beverage for 6 weeks. Fecal samples will be collected before and after each intervention to analyze microbiota composition using 16S rRNA sequencing. This study aims to characterize the gut microbiota of Paraguayan children for the first time and assess whether this functional beverage can positively modulate intestinal bacteria as a potential strategy to address childhood obesity, which affects 1 in 3 school-age children in Paraguay.

Interventions

  • Other Mango juice
    Mango juice drink for 6 weeks 200 ml daily, 5 days a week
  • Other Mango and chia juice
    Mango and chia juice drink for 6 weeks, 200 ml daily 5 days a week

Primary outcome measures

  • Microbiota [Time frame: Baseline and after 4 weeks]
Secondary outcome measures (1)
  • Anthropometric measurements [Time frame: Baseline and after 4 weeks]

Eligibility criteria

Inclusion criteria

100 children aged 8-16 years from Paraguay, stratified by BMI (with/without excess weight).

Exclusion criteria

Allergyc to mango or chia

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Supportive care

Study locations

Paraguay · 1 center
  • UNCA — Coronel Oviedo

Identifiers

NCT: NCT07529119 · PINV01-69

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗