Key Insights

Highlights

Success Rate

90% trial completion (above average)

Published Results

23 trials with published results (29%)

Research Maturity

62 completed trials (79% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

9.0%

7 terminated out of 78 trials

Success Rate

89.9%

+3.3% vs benchmark

Late-Stage Pipeline

29%

23 trials in Phase 3/4

Results Transparency

37%

23 of 62 completed with results

Key Signals

23 with results90% success

Data Visualizations

Phase Distribution

62Total
Not Applicable (37)
P 2 (2)
P 3 (6)
P 4 (17)

Trial Status

Completed62
Terminated7
Withdrawn5
Unknown3
Enrolling By Invitation1

Trial Success Rate

89.9%

Benchmark: 86.5%

Based on 62 completed trials

Clinical Trials (78)

Showing 20 of 20 trials
NCT06250322CompletedPrimary

A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens

NCT05574959Not ApplicableTerminatedPrimary

Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens, Model DEN00V

NCT05575063Not ApplicableCompletedPrimary

Clinical Investigation of Healon EndoCoat Ophthalmic Viscosurgical Device (OVD)

NCT06377514Not ApplicableCompletedPrimary

Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens

NCT05053399Not ApplicableCompletedPrimary

Evaluation of the TECNIS Symfony® Toric Intraocular Lens

NCT05531292Not ApplicableCompletedPrimary

PROOF-OF-CONCEPT STUDY FOR NEW INTRAOCULAR LENS, MODEL C0002

NCT05394324Completed

A Post-market Clinical Study to Collect Safety and Performance Data on Johnson & Johnson Surgical Vision Products

NCT05090826Not ApplicableCompletedPrimary

A Real-World Study for the TECNIS Synergy™ Intraocular Lens

NCT05090813Not ApplicableCompletedPrimary

A Real-World Study in China for the TECNIS Eyhance™ Intraocular Lens

NCT06005675CompletedPrimary

User Acceptability Evaluation of Pseudophakic Patients Previously Implanted With the TECNIS Odyssey IOL

NCT06257914Enrolling By InvitationPrimary

Aberrometry and Straylight Measurements as an Indication for Cataract Surgery

NCT05058274Completed

Clinical Results of a Monofocal Aspheric Bitoric Intraocular Lens With Plate Haptics in Hyperopic Eyes (HIPER-AT-TORBI)

NCT05991960CompletedPrimary

Evaluation of Real-World Data on the Performance of the TECNIS Odyssey™ IOL

NCT03409185Not ApplicableTerminatedPrimary

The Incidence of Glistenings in the 2017 Intraocular Lenses Made by Alcon and Abbott Medical Optics

NCT02487160Phase 3CompletedPrimary

Clinical Evaluation of the Lenstec SBL-3 Multifocal Intraocular Lens

NCT03708367Not ApplicableCompletedPrimary

A Post-Market Evaluation of LipiFlow Treatment in Cataract Surgery Practice

NCT01296191Phase 4CompletedPrimary

Aqueous Absorption and Pharmacokinetics of Besivance Versus VIGAMOX in Patients Undergoing Phacoemulsification

NCT01296542Phase 4CompletedPrimary

A Comparison of Prophylactic Antibacterial Efficacy of Besivance vs. VIGAMOX Prior to Cataract Surgery

NCT00342342CompletedPrimary

Family Studies of Eye Traits

NCT02691741Not ApplicableCompletedPrimary

Clinical Investigation of Visual Function After Bilateral Implantation of Two Presbyopia-Correcting Trifocal Intraocular Lenses (IOL)

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Research Network

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