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A prospective cohort study integrating multi-omics and brain imaging for the diagnosis and treatment of autism

A prospective cohort study integrating multi-omics and brain imaging for the diagnosis and treatment of autism

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101955
Enrollment
Unknown
Registered
2025-05-06
Start date
2025-02-21
Completion date
Unknown
Last updated
2025-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Autism Spectrum Disorder

Interventions

Control group:none

Sponsors

Children's Hospital,Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 17 Years

Inclusion criteria

Inclusion criteria: 1. According to clinical evaluation by a rehabilitation attending physician, it meets the DSM-5 diagnostic criteria for ASD; 2. ADOS assessment, consistent with ASD diagnosis; 3. Not receiving any psychotropic drugs in the past 3 months; 4. between 1-17 years old; 5. The child and parents agree to participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Other mental disorders that meet the DSM-5 criteria; 2. Currently participating in other clinical trials; 3. Diagnosed with Rett syndrome or fragile X syndrome through genetic testing or clinical diagnosis; 4. Patients with severe or unstable physical conditions, including cardiovascular diseases, tumors, kidney diseases, endocrine diseases (including thyroid dysfunction), gastrointestinal diseases, hematological diseases, and neurological diseases; 5. The researchers believe that there are other situations that are not suitable for participating in this study.

Design outcomes

Primary

MeasureTime frame
Brain function;Multi-omics;

Secondary

MeasureTime frame
Behavioral feature;

Countries

China

Contacts

Public ContactJinpiao Zhu

Children's Hospital,Zhejiang University School of Medicine

zhujinpiao@zju.edu.cn+86 571 81732401

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026