Innovative Medical

44 total trials 43 completed

Innovative Medical sponsors 44 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 43 completed. 41 of these trials are in Phase 3-4 (later-stage) and 0 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Cataracts, with 3 trials.

Trial Pipeline

44 total, page 1 of 1

COMPLETED Phase 4

Randomized Comparison of the Abbott WHITESTAR Signature System With Ellips Tranversal Ultrasound vs. the Alcon Infiniti With the Ozil Torsional Handpiece in Phacoemulsification: A Contralaterally-Controlled Trial

NCT01279031

COMPLETED Phase 4

Clear Corneal Incisions and Arcuate Incisions Utilizing FemtoSecond Laser Technology for Cataract Surgery

NCT01383057

COMPLETED Phase 4

Dispervise Ophthalmic Viscoelastic as an Agent to Ensure Watertight Wound Closure After Clear Corneal Cataract Incisions

NCT01298973

COMPLETED Phase 4

Laser Cataract Surgery With the Femtosecond Laser Technology

NCT01382823

COMPLETED Phase 4

Prospective Evaluation of Visual Outcomes With Tecnis One-Piece Multifocal Intraocular Lenses Compared With Patients Previously Implanted With Crystalens Aspheric Optic (AO)

NCT01191229

COMPLETED Phase 4

Evaluation of the Tecnis™ Multifocal and Crystalens™ Accommodating Intraocular Lenses

NCT01061281

COMPLETED

Comparative Study of Photopic and Mesopic Distance, Intermediate and Near Visual Acuity, and Spectacle Independence

NCT01191502

COMPLETED Phase 4

A Clinical Evaluation Pilot Study of the Efficacy of Blink® Tears Lubricant Eye Drops for the Relief of Dry Eye Symptoms Following Implantation of Tecnis® Multifocal Introcular Lens

NCT01061268

COMPLETED Phase 4

Evaluation of Outcomes Using the AMO Advanced Customvue™ iLasik Procedure

NCT01061294

COMPLETED Phase 4

An Evaluation of Outcomes Following Wavefront Optimized or Wavefront Guided Lasik Procedure in Low to Moderate Myopic Patients

NCT01173198

COMPLETED

An Open-Label Evaluation of Degree of Accommodation in Pseudophakic Patients Bilaterally Implanted With Monofocal Intraocular Lenses

NCT01004549

COMPLETED Phase 4

Evaluation Of Bilateral Tecnis Multifocal Versus ReSTOR 3D Intraocular Lenses

NCT01061918

COMPLETED

Prospective Health Assessment of Cataract Patients' Ocular Surface

NCT01016405

COMPLETED Phase 4

Topical Cyclosporine and Disease Progression

NCT00567983

COMPLETED Phase 4

Objective Measurements of Prolonged Effects of Restasis on Dry Eye Disease

NCT00567177

TERMINATED Phase 4

An Evaluation of Kinerase Pro+Therapy Regimen Vs. Kinerase Vs. Control for the Treatment of Skin Aging

NCT00492479

COMPLETED Phase 4

Oasys vs. Extreme H20 Xtra 59

NCT00477763

COMPLETED Phase 4

Safety and Efficacy of Optive in Contact Lens Wearers With Dry Eyes

NCT00469573

COMPLETED Phase 4

Refractive Surgery and Optive Compatibility Study

NCT00469157

COMPLETED Phase 4

Aqueous Concentrations and PGE2 Inhibition of Ketorolac 0.4% vs. Bromfenac 0.09% in Cataract Patients: Trough Drug Effects

NCT00469690

COMPLETED Phase 4

Evaluation of the Efficacy, Tolerability, and Patient Acceptance of Dermatix Q for the Prevention and Management of Scars

NCT00450775

COMPLETED Phase 4

Efficacy and Safety of a New Multi-dose Lubricant Eye Drop Concomitant With Restasis® (Cyclosporine A) for the Treatment of Dry Eye Symptoms

NCT00405457

COMPLETED Phase 4

Efficacy of Optive Versus Systane Concomitant With Restasis (Cyclosporine A) for the Treatment of Dry Eye Symptoms

NCT00399061

COMPLETED Phase 4

Efficacy of Cyclosporine for the Prevention and Treatment of Dry Eye Symptoms Following LASIK or Photorefractive Keratectomy

NCT00349440

COMPLETED Phase 4

Efficacy of Bimatoprost 0.03% in Patients Who Are Low-Responders to Latanoprost

NCT00347841

COMPLETED Phase 4

Ketorolac vs. Steroid in the Prevention of CME

NCT00348244

COMPLETED Phase 4

Comfort and Cleaning Evaluation of Multipurpose Solutions in Contact Lens Patients

NCT00519948

COMPLETED Phase 4

Bimatoprost Monotherapy vs. Dual Therapy With Travoprost and Timolol in Patients With Glaucoma and Ocular Hypertension

NCT00348023

COMPLETED Phase 4

Efficacy of Topical Cyclosporine 0.05% in the Prevention of Ocular Surface Inflammation Secondary to Pterygia

NCT00383396

COMPLETED Phase 4

Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining

NCT00483795

COMPLETED Phase 4

Comparison of Vitreous Levels of Acular LS 0.04%, Xibrom 0.09%, and Nevanac 0.1%

NCT00377546

COMPLETED Phase 4

Efficacy of Topical Ketorolac Versus Placebo for Improving Visual Outcomes Following Multifocal IOL Implantation

NCT00433225

COMPLETED Phase 4

Diurnal Curves With Bimatoprost 0.03% Versus Travoprost 0.004%

NCT00347802

COMPLETED Phase 4

Pilot Study Evaluation of 2 Artificial Tears. Evaluation of TBUT, Tear Meniscus Height and Tear Thickness

NCT00469521

COMPLETED Phase 4

Cross-Over Evaluation of Two Lubricating Eye Drops

NCT00493662

COMPLETED Phase 4

Comparison of Frequency of Use of Optive and Systane

NCT00406510

COMPLETED Phase 4

Efficacy of Topical Cyclosporine Versus Tears for Improving Visual Outcomes Following Multifocal IOL Implantation

NCT00349583

COMPLETED Phase 4

Therapeutic Variables in Cataract Surgery

NCT00407017

COMPLETED Phase 4

Acular LS vs. Nevanac in Post op Inflammation Following Cataract Surgery

NCT00348582

COMPLETED Phase 4

Comfort Evaluation of a New MPS vs. Replenish in Contact Lens Patients

NCT00518700

COMPLETED Phase 4

A Multicenter Evaluation of Methods to Reduce Hyperemia Associated With Bimatoprost Therapy for Glaucoma or Ocular Hypertension

NCT00348062

COMPLETED Phase 4

Brimonidine Purite 0.15% Versus Dorzolamide 2% Used as Adjunctive Therapy to Latanoprost

NCT00348400

COMPLETED Phase 4

Aqueous Concentrations and PGE2 Inhibition of Ketorolac 0.4% vs. Bromfenac 0.09% in Cataract Patients

NCT00347503

COMPLETED Phase 4

A Comparison of Optive in Patients Previously Using Systane for the Treatment of Dry Eye

NCT00399230

Phase Distribution

PhaseTrial count
Phase 4 41

What the Pipeline for Innovative Medical Shows

According to the ClinicalTrials.gov registry, Innovative Medical is linked to 44 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 43 are already marked complete, representing roughly 98% of the total.

The phase mix for Innovative Medical reports 41 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Innovative Medical is Cataracts with 3 linked trials, and 6 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.