Assessment of Vitamin D Level in Children With Autism in Assiut University Children Hospital
Vitamen D in Autism
1 other identifier
observational
50
0 countries
N/A
Brief Summary
In the present study, we aim to evaluate the serum level of 25 hydrxy vitamin D in autistic children .
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Sep 2023
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 26, 2023
CompletedFirst Posted
Study publicly available on registry
March 8, 2023
CompletedStudy Start
First participant enrolled
September 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2023
CompletedMarch 8, 2023
February 1, 2023
Same day
February 26, 2023
February 26, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Assessment of Vitamin D level in Children with Autism in assiut university children hospital
In the present study, we aim to evaluate the serum level of 25 hydrxy vitamin D in autistic children .
2 years
Interventions
Assessment of Vitamin D level in Children with Autism in assiut university children hospital
Eligibility Criteria
1. full history. 2. full clinical examination. 3. diagnosis of patients with ASD based on medical experience,clinical examination and two criteria of DSM-IV . 4. evaluation of serum 25 hydroxy vitamin D level ; 5 ml of venous blood sample is taken for the test.
You may qualify if:
- Patient who full filled the diagnostic criteria of autism spectrum disorder according to DSM-IV.
You may not qualify if:
- )Children using vitamin D supplement. 2)patients with associated congenital malformation. 3)patients with chromosomal abnormalities. 4)patients with chronic physical illness. 5)patients with epilepsy. 6)patients with hepatic or renal disease.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Links
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- assiutU
Study Record Dates
First Submitted
February 26, 2023
First Posted
March 8, 2023
Study Start
September 1, 2023
Primary Completion
September 1, 2023
Study Completion
December 1, 2023
Last Updated
March 8, 2023
Record last verified: 2023-02