- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07687797
Partially Hydrolysed Whey Based Formula in Differentiation Between Non IgE Gastrointestinal Cow's Milk Protein Allergy and Milk Intolerance
June 30, 2026 updated by: Mostafa Elhodhod, Ain Shams University
Partially hydrolysed whey based formula in differentiation between non IgE gastrointestinal cow's milk protein allergy and milk intolerance
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Mostafa Elhodhod
- Phone Number: +2010065541445
- Email: moshodhod@med.asu.edu.eg
Study Locations
-
-
-
Cairo, Egypt, 11566
- Faculty of Medicine Ain Shams University
-
Contact:
- Fatma Ebeid
- Phone Number: 01095569596
- Email: dr.fatma_ebeid@yahoo.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- 1-6 months of age
- formula fed infants
- CoMiSS score above 10
- Repeated body mucoid stool
Exclusion Criteria:
- IgE mediated disease
- Skin allergy
- Respiratory symptoms
- Exclusive or mixed breast feeding
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: classic algorithm pathway receiving amino acid based formula
study pathway receiving partially hydrolyzed whey based formula
|
classic pathway of cow milk protein intolerance
|
|
Experimental: study pathway receiving partially hydrolyzed whey based formula
|
partially hydrolysed whey based formula
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
determining the frequency of cow milk intolerance diagnosis among patients suspected for cow milk protein allergy
Time Frame: 12 weeks
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
August 1, 2026
Primary Completion (Estimated)
August 1, 2027
Study Completion (Estimated)
December 1, 2027
Study Registration Dates
First Submitted
June 30, 2026
First Submitted That Met QC Criteria
June 30, 2026
First Posted (Actual)
July 7, 2026
Study Record Updates
Last Update Posted (Actual)
July 7, 2026
Last Update Submitted That Met QC Criteria
June 30, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- FMASU R115/2026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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