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CORNEAL biomechanics in subjects with posterior FOVEA

CORNEAL biomechanics in subjects with posterior FOVEA

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100041650
Enrollment
Unknown
Registered
2021-01-01
Start date
2020-12-30
Completion date
Unknown
Last updated
2021-03-22

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

Conditions

Posterior FOVEA OF IRIS

Interventions

RETROFOVEA group and normal group:Nil

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 51 Years

Inclusion criteria

Inclusion criteria: 1.Control group inclusion criteria: A. Age over 18 years old, no subjective symptoms of eye discomfort, UBM examination without Iris Fovea; B. All participants signed an informed consent form when they volunteered for the study. 2.Participants'inclusion criteria: A. Age over 18 years old, no subjective symptoms of eye discomfort, UBM examination of Iris Fovea; B. All participants signed an informed consent form when they volunteered for the study.

Exclusion criteria

Exclusion criteria: (1) Patients who have undergone eye surgery and suffer from other eye diseases such as Glaucoma and Iritis; (2) Patients with ocular surface abnormalities such as eyelid insufficiency, active phase of infectious Keratitis, having Human Herpesvirus 1 Keratitis, trigeminal nerve disease, and other known conditions that affect the biomechanics of the cornea; (3) Intraocular pressure above 21 mmhg.

Design outcomes

Primary

MeasureTime frame
Posterior FOVEA OF IRIS;

Countries

China

Contacts

Public ContactJunhua Li

Zhejiang Eye Hospital

674321334@qq.com+86 15888711134

Outcome results

None listed

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