Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

0.0%

0 terminated out of 29 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

34%

10 trials in Phase 3/4

Results Transparency

33%

6 of 18 completed with results

Key Signals

6 with results100% success

Data Visualizations

Phase Distribution

24Total
Not Applicable (12)
P 1 (2)
P 3 (4)
P 4 (6)

Trial Status

Completed18
Unknown6
Withdrawn3
Enrolling By Invitation1
Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 18 completed trials

Clinical Trials (29)

Showing 20 of 20 trials
NCT07317661Not ApplicableEnrolling By Invitation

Effectiveness of a Large Language Model-Based Educational Tool on Intraocular Lens Options

NCT07305987Phase 3RecruitingPrimary

PRO-232 in Patients Subjected to Cataract Surgery

NCT05571683CompletedPrimary

Cerebral Oxymeter and End Tidal Carbondioxide Values Under Surgical Drapes With and Without Past COVID-19 Infection

NCT02332369Not ApplicableUnknownPrimary

EyeKon Medical Inc. Capsular Tension Ring Study

NCT04977115Not ApplicableUnknownPrimary

Clinical Evaluation of Intraocular Caliper-assisted Capsulotomy for Age-related Cataract

NCT04977102Not ApplicableUnknownPrimary

A Randomized Study of Intraocular Caliper-assisted Capsulotomy for Age-related Cataract Patients With Corneal Limbus Opacity

NCT00708331Not ApplicableWithdrawnPrimary

Hydrophilic Acrylic Intraocular Lens

NCT03364972Not ApplicableCompletedPrimary

A Study Comparing Two Monofocal, Aspheric, Hydrophobic Acrylic Intraocular Lenses: the Alcon CLAREON® and the Abbott Medical Optics PCB00

NCT03944070Not ApplicableUnknown

Management of Patients With Neovascular Age-related Macular Degeneration Undergoing Cataract Surgery

NCT03828500Not ApplicableUnknownPrimary

Preoperative Fasting for Ambulatory Cataract Surgery: The PRACTICE Study

NCT02973880Phase 3CompletedPrimary

Clinical Study to Evaluate the Efficacy and Tolerability of an Anti-inflammatory/Antibiotic Treatment Following Ocular Cataract Extraction

NCT00366613Phase 4WithdrawnPrimary

Clinical Evaluation of the Use of Sealed Capsule Irrigation With Sodium Chloride During Pediatric Cataract Surgery and IOL Implantation

NCT00366691Phase 4CompletedPrimary

Comparison of Acular LS With Lotemax to Prevent Inflammation After Cataract Surgery and Intraocular Lens Implantation

NCT00366587Phase 4CompletedPrimary

Comparison of Visual Outcomes and Patient Satisfaction After Cataract Surgery and Implantation of ReSTOR and ReZoom IOLs

NCT00466908WithdrawnPrimary

Accuracy of the Pentacam and IOL Master to Calculate the Effective Corneal Power After Corneal Refractive Surgery

NCT00924729Phase 4CompletedPrimary

Study of Ocular Penetration of Topically Administered Fluoroquinolones

NCT01198483Not ApplicableUnknownPrimary

Microincision Versus Smallincision Combined Surgery

NCT00721695Phase 1CompletedPrimary

Exploratory Study of OMS302 Injection in Subjects Undergoing Unilateral Cataract Extraction by Phacoemulsification.

NCT00840580Phase 4CompletedPrimary

Effect on Wound Healing of Vigamox Versus Cravit

NCT00824070Phase 1CompletedPrimary

Assessment of the Concentrations of Besifloxacin, Moxifloxacin, or Gatifloxacin in the Aqueous Humor of Subjects

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