- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06441734
Iron Status in Autism Spectrum Disorders
July 15, 2024 updated by: esraa hefzy shaker mostafa, Assiut University
Iron Status in Autism Spectrum Disorders in Children Attending Assiut Pediatric University Hospital
to evaluate the prevalence of iron deficiency anemia in group with autism spectrum disorders in comparison to normal children group
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
46
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: esraa hefzy shaker
- Phone Number: 01090930692
- Email: esraahefzy31@gmail.com
Study Contact Backup
- Name: emad eldeen mahmoud hammad, professor
- Phone Number: 01223559943
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
N/A
Sampling Method
Non-Probability Sample
Study Population
children age from 2years to 12 years not having an infection or inflammatory conditions or physical illness
Description
Inclusion Criteria:
- children who are diagnosed with autism spectrum disorder according to DSM -V
- not having infection inflammatory conditions chronic physical illness
- children who are not receiving iron supplementation
Exclusion Criteria:
- age below 2 years and above 12 years
- having an infection or inflammatory conditions chronic physical illness
- receiving iron supplementation
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
control group
|
by using sample of blood to do cbc and serum ferritin and serum iron during 1year
|
|
study group
|
by using sample of blood to do cbc and serum ferritin and serum iron during 1year
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
iron status in autism spectrum disorders
Time Frame: 1 year
|
by cbc serum ferritin serum iron
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: khalaf abdelaal said, lecturer, Assiut University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
Helpful Links
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 2, 2024
Primary Completion (Estimated)
June 2, 2025
Study Completion (Estimated)
July 1, 2025
Study Registration Dates
First Submitted
May 29, 2024
First Submitted That Met QC Criteria
June 3, 2024
First Posted (Actual)
June 4, 2024
Study Record Updates
Last Update Posted (Actual)
July 16, 2024
Last Update Submitted That Met QC Criteria
July 15, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- anemia in autism
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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