Pure Global

The Effect of Continuous Egg Supplement on Personalized Nutri-omics in Primary School Children (SI-EGG STUDY) - Trial NCT04896996

Access comprehensive clinical trial information for NCT04896996 through Pure Global AI's free database. This phase not specified trial is sponsored by Mahidol University and is currently Completed. The study focuses on Malnutrition, Child. Target enrollment is 635 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

Free Database
Powered by Pure Global AI
840K+ Trials
NCT04896996
Completed
dietary supplement
Trial Details
ClinicalTrials.gov โ€ข NCT04896996
View on ClinicalTrials.gov
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
The Effect of Continuous Egg Supplement on Personalized Nutri-omics in Primary School Children (SI-EGG STUDY)

Study Focus

Malnutrition, Child

whole eggs

Interventional

dietary supplement

Sponsor & Location

Mahidol University

Bangkok Noi, Thailand

Timeline & Enrollment

N/A

May 21, 2019

Apr 29, 2020

635 participants

Primary Outcome

changes in body weight following the dietary intervention,changes in height following the dietary intervention,change in blood protein levels following dietary intervention,changes in blood biochemistries following dietary intervention

Summary

This research compares the effects of one-year continuous whole egg supplement vs. egg yolk
 substitutes and control on anthropometry, biochemical blood parameters, metabolic enzymes and
 microbiome data in primary school children.

ICD-10 Classifications

Malnutrition
Malnutrition in pregnancy
Sequelae of malnutrition and other nutritional deficiencies
Malnutrition-related diabetes mellitus
Malnutrition-related diabetes mellitus with unspecified complications

Data Source

ClinicalTrials.gov

NCT04896996

Non-Device Trial