a comparative study of pupillary offset measurement using pentacam and keratron scout in myopia

Status

Active, not recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200060181

Enrollment

Unknown

Registered

2022-05-21

Start date

2022-05-09

Completion date

Unknown

Last updated

2024-04-29

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

Conditions

Refractive errors

Interventions

pentacam group:None

keratronscout group:None

Eligibility

Sex/Gender

All

Age

18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years; 2. The diopter is basically stable for more than 2 years; 3. Stop wearing soft contact lenses for at least 2 weeks and hard orthokeratology lenses for at least 4 weeks before surgery, and the corrected vision is normal; 4. Spheroscope less than 1000.

Exclusion criteria

Exclusion criteria: 1. There was active inflammation of the eye, periocular purulent, and serious lesions of accessory organs of the eye; 2. Associated with glaucoma, keratoconus, systemic connective tissue diseases; 3. Accompanied by mental diseases, diabetes, systemic infectious diseases or autoimmune diseases.

Design outcomes

Primary

Measure	Time frame
pupillary offset;	—

Countries

China

Contacts

Public ContactHuang Yue

1097813271@qq.com+86 15620662542

Outcome results

None listed

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