- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06494852
Association of Renal-tubular Acidosis in Children With Cow Milk Protein Allergy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a cross-sectional study that will be conducted over 6 months at the pediatric department, Sohag University Hospital, Sohag, Egypt.
Children proved to be with cow milk protein allergy by oral challenge test after stabilization and prevention of cow protein with Age group from 3 months up to 3 years attending outpatient clinic at Sohag University Hospital will be included in the study.
The study participants will be subjected to full history taking and thorough clinical examination at the pediatric outpatient clinic and their medical files will be reviewed.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Sohag, Egypt
- Sohag
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Children proved to be with cow milk protein allergy by oral challenge test after stabilization and prevention of cow protein with Age group from 3 months up to 3 years attending outpatient clinic at Sohag University Hospital will be included in the study
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
investigate association of Renal tubular acidosis in cow milk protein allergy patients
Time Frame: 6 months
|
Our study aims to detect renal manifestations of children proved to be with cow milk protein allergy special focusing on tubular dysfunction
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6 months
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Metabolic Diseases
- Immune System Diseases
- Kidney Diseases
- Urologic Diseases
- Hypersensitivity, Immediate
- Genetic Diseases, Inborn
- Renal Tubular Transport, Inborn Errors
- Acid-Base Imbalance
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Hypersensitivity
- Milk Hypersensitivity
- Food Hypersensitivity
- Acidosis
- Acidosis, Renal Tubular
Other Study ID Numbers
- Soh-Med-24-5-02MS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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