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Research on iPSCs and organoids related to genetic mutation-associated neurodevelopmental disorders in chlidren

Research on iPSCs and organoids related to genetic mutation-associated neurodevelopmental disorders in chlidren

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116294
Enrollment
Unknown
Registered
2026-01-08
Start date
2026-01-31
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

neurodevelopmental disabilitie

Interventions

Patients with neurodevelopmental disorders:NA

Sponsors

The First Medical Center of the Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 14 Years

Inclusion criteria

Inclusion criteria: (1) The department has at least two NDD patients with the same gene mutation; (2) Patients meet the diagnostic criteria for neurodevelopmental disorders (NDD); (3) Patients and their family members cooperate with the collection of biological samples; (4) Aged 0 to 14 years (inclusive), both males and females are eligible.

Exclusion criteria

Exclusion criteria: (1) Patients or their family members who refuse to cooperate with blood collection; (2) Patients with other neurological diseases in addition to neurodevelopmental disorders (NDD); (3) Other circumstances deemed unsuitable for enrollment by the researchers.

Design outcomes

Primary

MeasureTime frame
Constructing brain organoids;

Countries

China

Contacts

Public ContactYang Guang

The First Medical Center of the Chinese PLA General Hospital

675779839@qq.com+86 152 8550 5367

Outcome results

None listed

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