Condition
Contact Lens-Induced Corneal Fluorescein Staining
Total Trials
4
Recruiting
0
Active
0
Completed
3
Success Rate
100.0%+13% vs avg
Key Insights
Highlights
Success Rate
100% trial completion (above average)
Clinical Risk Assessment
Based on trial outcomes
Moderate Risk
Score: 50/100
Termination Rate
0.0%
0 terminated out of 4 trials
Success Rate
100.0%
+13.5% vs benchmark
Late-Stage Pipeline
0%
0 trials in Phase 3/4
Results Transparency
33%
1 of 3 completed with results
Key Signals
1 with results100% success
Data Visualizations
Phase Distribution
3Total
Not Applicable (2)
P 2 (1)
Trial Status
Completed3
Not Yet Recruiting1
Trial Success Rate
100.0%
Benchmark: 86.5%
Based on 3 completed trials
Clinical Trials (4)
Showing 4 of 4 trials
NCT06351410Not ApplicableNot Yet Recruiting
Assessment of Tear Production, Corneal Staining, and Comfort Level Wearing Different Types of Contact Lenses
NCT03994406Phase 2Completed
Prolongation of Contact Lens Comfortable Wear Duration by CLM2 Topical Gel
NCT01015768Not ApplicableCompletedPrimary
Corneal Staining and Physiological Compromise After Eight Hours of Soft Contact Lens Wear
NCT03305484Completed
Soft Contacts Observation of Risk and Education (SCORE)
Showing all 4 trials