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Neonatal eyeball parameter measurement

Neonatal eyeball parameter measurement

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000031628
Enrollment
Unknown
Registered
2020-04-05
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-04-06

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

Conditions

Natural development

Interventions

The group of premature infants without ROP disease, the group of ROP does not need laser treatment, the group of ROP requiring laser treatment and the group of term infants:N/A

Sponsors

Wenzhou Medical University Affiliated Optometry Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Premature and full term infants.

Exclusion criteria

Exclusion criteria: In addition to ROP, other organic diseases of the eye, including congenital cataract, congenital glaucoma, congenital small eyeball, neonatal macular area bleeding, and other systemic conditions can not tolerate the examination of premature infants or full months.

Design outcomes

Primary

MeasureTime frame
axial length;cornea thickness;diopter;Intraocular pressure;—

Countries

China

Contacts

Public ContactJianbo Mao

Wenzhou Medical University Affiliated Optometry Hospital

rocket222@sina.com+86 15868400490

Outcome results

None listed

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