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Clinical Characteristics and Genetic Analysis of Ocular Diseases in Children with Craniosynostosis

Clinical Characteristics and Genetic Analysis of Ocular Diseases in Children with Craniosynostosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600124207
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-31
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Craniosynostosis

Interventions

Sponsors

Shanghai Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Children diagnosed with craniosynostosis; 2. Suffering from eye diseases, including one or more of the following: strabismus, ptosis, inverted eyelashes, refractive errors, fundus diseases, eye hernias, etc; 3. Sign informed consen.

Exclusion criteria

Exclusion criteria: 1.Non congenital eye diseases, such as secondary eye diseases caused by trauma or tumors; 2.Unable to comply with research or follow-up procedures; 3.Patients with serious systemic diseases who cannot undergo eye examinations or surgeries; 4.Researchers believe that those who need to be excluded.

Design outcomes

Primary

MeasureTime frame
Diopter;Strabismus;

Secondary

MeasureTime frame
Muscle strength of the upper eyelid muscle;

Countries

China

Contacts

Public ContactLiu Qingyu

Shanghai Children's Hospital

drlqy2013@163.com+86 137 6465 4420

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026