Key Insights

Highlights

Success Rate

98% trial completion (above average)

Published Results

26 trials with published results (49%)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 37/100

Termination Rate

1.9%

1 terminated out of 53 trials

Success Rate

97.8%

+11.3% vs benchmark

Late-Stage Pipeline

4%

2 trials in Phase 3/4

Results Transparency

58%

26 of 45 completed with results

Key Signals

26 with results98% success

Data Visualizations

Phase Distribution

47Total
Not Applicable (44)
P 2 (1)
P 3 (1)
P 4 (1)

Trial Status

Completed45
Recruiting3
Active Not Recruiting2
Not Yet Recruiting1
Terminated1
Withdrawn1

Trial Success Rate

97.8%

Benchmark: 86.5%

Based on 45 completed trials

Clinical Trials (53)

Showing 20 of 20 trials
NCT07557030Not ApplicableNot Yet Recruiting

Optimization for Toric Contact Lenses

NCT07104773Not ApplicableCompletedPrimary

Clinical Investigation of Proclear® 1 Day and MyDay® Sphere Contact Lenses

NCT07375589Not ApplicableCompleted

LED Low-Intensity Red Light for Myopia Control in Youth: Efficacy and Safety Study

NCT07168564Not ApplicableRecruitingPrimary

Post Marketing Clinical Study on the Efficacy of Lenses From a New Prescription Protocol

NCT06902584Recruiting

North American Comfilcon A Clinical Study

NCT06400914Not ApplicableCompletedPrimary

Clinical Evaluation of Biomedics Monthly Sphere and Avaira Vitality Sphere

NCT06408649TerminatedPrimary

Post-market Clinical Follow-up Study of Alcon TOTAL30® Contact Lenses (Lehfilcon A)

NCT06165627Not ApplicableCompletedPrimary

Comparison of Clinical Performance of Two Monthly Replacement Toric Soft Contact Lenses

NCT06882408Not ApplicableRecruitingPrimary

The Objective of This Study is to Evaluate the Perfomance of a Photorefraction Device for Screening Ametropia in Children. Eligible Participants Will Undergo Multiple Refractive Error Measurements, Visual Acuity and Strabismus Assessments During a Single Evaluation Visit.

NCT06524115Not ApplicableCompletedPrimary

Optimization of a Photoretinoscopy Method for Determining the Objective Refraction of Children With a Smartphone/add-on Device in India

NCT06295536Not ApplicableCompletedPrimary

Optimization of a Photoretinoscopy Method for Determining the Objective Refraction of Children

NCT04632784Not ApplicableActive Not Recruiting

Clinical Trial With Artiflex Presbyopic (Artiplus)

NCT05959200Not ApplicableCompletedPrimary

Clinical Performance Evaluation of Two Frequent Replacement Silicone Hydrogel Toric Contact Lenses

NCT06668246Active Not Recruiting

Performance of Refractometers With Self-adjusting Lenses Compared to Cycloplegia in Children (REFRALENS)

NCT06642779Completed

Comparative Analysis of the Visual Performance and Patient Satisfaction After Cataract Surgery With Implantation of a Medicontur Monofocal (877PAY) or a Medicontur Extended Depth of Focus (877PEY) IOL

NCT04714424Completed

Comparing Vision Tests in a Virtual Reality Headset to Existing Analogues

NCT04617080Not ApplicableCompletedPrimary

Safety and Efficacy of Different Add Powers With a New Presbyopic Lasik Treatment Algorithm

NCT05516082Not ApplicableCompletedPrimary

Clinical Evaluation of Two Daily Disposable Lenses in Sphere Design

NCT04185701Not ApplicableCompleted

Comparison of Subjective Refraction Measurement With SiVIEW Software and by an Expert

NCT05483127Not ApplicableCompleted

Clinical Comparison of Two Daily Disposable Toric Soft Contact Lenses

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