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New treatment of keratoconus with UV

comparison of 30 minutes and 5 minutes collagen cross-linking in patients with keratoconus

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201207244333N1
Enrollment
60
Registered
2012-08-30
Start date
2012-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Keratoconus. keratoconus

Interventions

Intervention 1: Intervention name: 5 min-UV radiation in corneal cross-linking Intervention description: After local anesthesia with Proparacaine hydrochloride 0.5% eye drop, 3 or 4 vertical strips ab
Treatment - Surgery
Intervention name: 5 min-UV radiation in corneal cross-linking Intervention description: After local anesthesia with Proparacaine hydrochloride 0.5% eye drop, 3 or 4 vertical strips about 2 mm wide r
The control intervention: 30 min-UV radiation in corneal cross-linking (routin treatment) Control intervention description: After local anesthesia with Proparacaine hydrochloride 0.5% eye drop, 3 or

Sponsors

Noor eye hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 35 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: keratometry less than 60 diopter; central corneal thickness of 400 microns or more; keratoconus progression in the past 12 months documented as at least one D increase in maximum keratometry, or manifest cylinder; Bilateral surgery Exclusion criteria: diabetes and other systematic disease; use of corticosteroid and immunosupressive drugs in the past 6 months

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Corneal biomechanical assay. Timepoint: pre op, 1m, 3m and 6m after surgery. Method of measurement: Cornea status is evaluated by Ocular Response Analyzer (ORA), confoscan, and endothelial cell count (ECC).

Secondary

MeasureTime frame
Refraction. Timepoint: pre op, 1m, 3m and 6m after surgery. Method of measurement: autorefractometer.;Keratometry. Timepoint: pre op, 1m, 3m and 6m after surgery. Method of measurement: Pentacam.;Visual acuity. Timepoint: pre op, 1m, 3m and 6m after surgery. Method of measurement: Snellen chart.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSoheila Asgari

Noor eye hospital

soheilaasgari@gmail.com+98 21 8240 1621

Outcome results

None listed

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