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Clinical observation of keratoconus in Chinese population

Clinical observation of keratoconus in Chinese population

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100051067
Enrollment
Unknown
Registered
2021-09-11
Start date
2013-01-01
Completion date
Unknown
Last updated
2022-05-16

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

Conditions

Keratoconus

Interventions

case series:Nil

Sponsors

Eye and ENT Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with a clinical diagnosis of keratoconus in one or both eyes. 2. Any age limit. 3. Patients with no active ocular disease.

Exclusion criteria

Exclusion criteria: 1. Presence of an eye infection. 2. Patients who have taken antipsychotic and antidepressant medication within the last six months or are taking them. 3. Those who have undergone internal eye surgery. 4. Those who have had severe corneal disease. 5. Women who are pregnant or breastfeeding or planning to become pregnant at the time of the clinical study. 6. Those who, in the judgment of the investigator, are unable to understand or cooperate with the procedures of this study. 7. Participating in another clinical trial within 30 days prior to the conduct of this study. 8. Patients with only one eye.

Design outcomes

Primary

MeasureTime frame
Visual acuity;corneal tomography;Corvis ST;

Countries

China

Contacts

Public ContactZhou Xingtao

Eye and ENT Hospital of Fudan University

doctzhouxingtao@163.com+86 13816880725

Outcome results

None listed

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