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NOT YET RECRUITING
NCT06588036
EARLY_PHASE1

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

Sponsor: Combined Military Hospital Multan

View on ClinicalTrials.gov

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.

Official title: A Comprehensive Analysis of the Comparative Efficacy of Multimodal Diarrhea Therapies

Key Details

Gender

All

Age Range

6 Months - 5 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2024-09-15

Completion Date

2024-12-30

Last Updated

2024-09-19

Healthy Volunteers

No

Interventions

DRUG

Prebiotic

. 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.

OTHER

Duration

every participant is alloted a group based on RCT.

DRUG

Smecta

Group 4 will be given smecta scahet