Skip to content

Multicenter Genetic Study of Keratoconus Families?

Multicenter Genetic Study of Keratoconus Families?

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125085
Enrollment
Unknown
Registered
2026-05-21
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

keratoconus

Interventions

Case Group:None

Sponsors

Eye Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 45 Years

Inclusion criteria

Inclusion criteria: 1. The proband must have at least one eye diagnosed with primary keratoconus; 2. The family pedigree must include at least the proband and both parents (a minimum of 3 participants); 3. All participating family members have agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. The proband is diagnosed with non-primary keratoconus, e.g., secondary keratoconus; 2. The number of participating family members is insufficient to meet the study requirements; 3. The clinical data or biological samples from the family participants are missing, failing to meet the study requirements.

Design outcomes

Primary

MeasureTime frame
genetic locus;corneal signs, corneal topography, corneal biomechanics;

Countries

China

Contacts

Public ContactShihao Chen

Eye Hospital, Wenzhou Medical University

csh@eye.ac.cn+86 577 88068862

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026