drugset / Trial / NCT06588036

A Comprehensive Analysis of the Comparative Efficacy of Multimodal Diarrhea Therapies in the Paediatric Population

NCT06588036

RandomizedSingle-groupSingle-blindTreatment

Summary

The objective of this research is to assess the mean time of resolution of diarrhea in pediatric patients receiving different intervention combinations for the management of acute diarrhea. Specifically, the study aims to compare the effectiveness of four intervention groups: Group 1 receiving zinc and probiotic supplementation, Group 2 receiving zinc, probiotic, and prebiotics. Group 3 receiving zinc, probiotics, and anti-secretory agents, and Group 4 receiving zinc, probiotic, anti-secretory agents, and adsorbents. The primary outcome measure will be the mean time from the initiation of treatment to the resolution of diarrhea symptoms. This objective seeks to provide evidence-based insights into the optimal management strategies for childhood diarrhea and inform clinical practice guidelines.

Timeline

Start
2024-09-15
Primary completion
2024-12-15
Completion
2024-12-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator montmorillonite Other / unclassified
Comparator Zinc Sulfate Unknown

Indications

No indication recorded.