Trials / Recruiting
RecruitingNCT03922542
Comparison of Standard vs. Accelerated Corneal Crosslinking
Randomized Comparison of Standard vs. Accelerated Corneal Crosslinking for Treatment of Progressive Keratoconus or Ectasia
- Status
- Recruiting
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 510 (estimated)
- Sponsor
- Price Vision Group · Industry
- Sex
- All
- Age
- 10 Years
- Healthy volunteers
- Not accepted
Summary
The study objective is to compare accelerated and standard corneal crosslinking for treatment of progressive keratoconus or corneal ectasia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| COMBINATION_PRODUCT | riboflavin 0.1% | Use of riboflavin 0.1% eye drops and 9 mW/cm2 UVA light for 10 minutes |
| COMBINATION_PRODUCT | Riboflavin 0.1% | Use of riboflavin 0.1% eye drops and 3 mW/cm2 UVA light for 30 minutes |
Timeline
- Start date
- 2019-04-16
- Primary completion
- 2026-06-01
- Completion
- 2026-07-01
- First posted
- 2019-04-22
- Last updated
- 2025-07-31
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03922542. Inclusion in this directory is not an endorsement.