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Evaluation of corneal crosslinking in progressive keratoconus

Evaluation of corneal crosslinking in progressive keratoconus - Evaluation of corneal crosslinking

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025012
Enrollment
100
Registered
2016-12-01
Start date
2011-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

keratoconus

Interventions

Sponsors

Nagoya Eye Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Increase in Steepest K-value more than 1.0D 2. Increase in manifest cylinder more than 1.0D 3. Increase in manifest spherical equivalent more than 1.0D One of the above conditions was found within 24 months and the thinnest corneal thickness is 400 um or more.

Exclusion criteria

Exclusion criteria: The corneal thickness is less than 400 um . Those who is implanted cardiac pacemaker, or other medical devices Non of the conditions below are observed; 1 Increase in Steepest K-value more than 1.0D 2 Increase in manifest cylinder more than 1.0D 3 Increase in manifest spherical equivalent more than 1.0D Those who have ocular disorders, such as infections, scars, ocular herpes, nystagmus etc. those who have general diseases that can affect the corneal wound healing Narrow angle Those who is in pregnancy or breast-feeding Occupations that are not allowed to undergo refractive surgeries Age less than 14 year-old

Design outcomes

Primary

MeasureTime frame
visual acuity, manifest visual acuity, corneal thickness, corneal higher order aberrations

Countries

Japan

Contacts

Public ContactJunko Sawada

Nagoya Eye Clinic Ethics committee

nic-irb@lasik.jp0120-758-049

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026