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NCT06673082 | NOT YET RECRUITING | Cow Milk Protein Allergy


Impact of Zinc As a New Adjuvant Therapy for Cow Milk Protein Allergy in Children.
Sponsor:

Kasr El Aini Hospital

Information provided by (Responsible Party):

Arwa Ahmed

Brief Summary:

Children presented with manifestations of Cow Milk Protein Allergy will be enrolled for Cow Milk -related Symptoms Score (CoMiSS assessment). Detailed History, nutritional and clinical examination will be done to fulfill items of CoMiSS. Children will be randomly allocated to two groups. Oral Zinc will be supplemented to the interventional group. CoMiSS will be recorded at the baseline and weekly till 4 weeks. Then Oral Food Challenge (OFC) will be done to confirm the diagnosis and CoMiSS assessment will be recorded again to see if Zinc has any modulatory effect on reappearance of symptoms. The people administering the intervention, the people assessing the outcomes, the patients and their caregivers will all be blinded to the type of treatment. Children who will be presented with skin manifestation will be assessed by Severity Scoring of Atopic Dermatitis Index (SCORAD score) once diagnosed and weekly till 4 weeks after zinc supplementation to see if Zinc has any modulatory effect.

Condition or disease

Cow Milk Protein Allergy

Intervention/treatment

Oral zinc supplementation

Placebo

Phase

NA

Detailed Description:

Children who will be presented with manifestations of Cow Milk Protein Allergy will be enrolled in the study for Cow Milk -related Symptoms Score (CoMiSS) assessment. Detailed History, nutritional and clinical examination will be done to fulfill items of CoMiSS including skin manifestations as eczema , respiratory manifestations, GIT manifestations as constipation or diarrhea including Bristol scale and regurgitations and duration of crying . Children will be randomly allocated to two groups. Randomization will be done using GraphPad QuickCalcs software to allocate into either the interventional or control group. Oral Zinc will be supplemented to the interventional group on adose of 30 mg elemental zinc/day. CoMiSS will be recorded at the baseline and weekly till 4 weeks. Then Oral Food Challenge (OFC) will be done to confirm the diagnosis and CoMiSS assessment will be recorded againto see if Zinc has any modulatory effect on reappearance of symptoms. The people administering the intervention, the people assessing the outcomes, the patients and their caregivers will all be blinded to the type of treatment. Children who will be presented with skin manifestation will be assessed by Severity Scoring of Atopic Dermatitis Index (SCORAD score) once diagnosed and weekly till 4 weeks after zinc supplementation to see if Zinc has any modulatory effect.

Study Type : INTERVENTIONAL
Estimated Enrollment : 190 participants
Masking : QUADRUPLE
Primary Purpose : OTHER
Official Title : Impact of Zinc As a New Adjuvant Therapy for Cow Milk Protein Allergy in Children, a Randomized Controlled Trial
Actual Study Start Date : 2024-12-01
Estimated Primary Completion Date : 2025-04-15
Estimated Study Completion Date : 2025-05-15

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 1 Month to 12 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • Children suspected to have Cow Milk Protein Allergy using Cow's Milk-relatedSymptoms Score with a Score more than12 Age less than 12 years old both sexes Whose parents approved to be enrolled in the study
Exclusion Criteria
  • Children with Comorbidities that may affect the duration of treatment as dysphagia.
  • History of Severe allergic reaction that required hospital admission as Ora Food Challenge is expectedto be delayed in these patients.
  • -Multiple Food Allergies

Impact of Zinc As a New Adjuvant Therapy for Cow Milk Protein Allergy in Children.

Location Details

NCT06673082


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Locations


Not yet recruiting

Egypt,

faculty of medicine-Cairo universty

Giza, Egypt, 12556

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