Vance Thompson Vision

Sioux Falls, South Dakota 57108

3 studies enrolling now · 57 studies all time

What they study most

Aphakia, Astigmatism, Blepharoplasty, Cataract, Cataracts, Corneal Astigmatism, Corneal Ectasia, Corneal Edema, Corneal Edema After Cataract Surgery, Dry Eye, Dry Eye Syndromes, Glaucoma

Studies at this site

• Evaluating Patient Reported Outcomes and Surgeon Satisfaction With Ziplyft™ — Recruiting now
• A Study to Evaluate Efficacy and Safety of MELT-300 for Procedural Sedation in Subjects Undergoing Cataract Extraction With Lens Replacement (CELR) — Recruiting now
• Contoura With Phorcides Compared to Wavefront Optimized LASIK — Recruiting now
• A Study to Investigate the Safety and Efficacy of Ripasudil (K-321) Eye Drops After Cataract Surgery — Completed
• Wavefront-guided LASIK for Monovision Treatment of Myopic Subjects With Presbyopia — Completed
• Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens — Completed
• Study to Evaluate the Safety and Efficacy of CSB-001 Ophthalmic Solution 0.1% in Neurotrophic Keratitis Subjects — Completed
• Exploring Sedation Types During Cataract Surgery — Completed
• Use of the VisuMax™ Femtosecond Laser — Completed
• Multicenter Clinical Trial of a Phakic Implantable Collamer® Lens (ICL) — Completed
• Post-Market Evaluation of the EVO ICL — Completed
• Evaluation of Clareon Vivity/Vivity Toric — Completed
• Clinical Trial of a Hydrophilic EMV Toric Lens RAO210T in the Correction of Aphakia and Corneal Astigmatism — Completed
• A Cataract Surgery Clinical Trial — Withdrawn before enrolling
• Safety And Effectiveness Of The TearCare® System In The Treatment Of The Signs And Symptoms Of Dry Eye Disease (SAHARA) — Completed
• TearCare System to Treat Dry Eye Disease — Completed
• Randomized Study of the Safety and Effectiveness of the TearCare System for the Signs and Symptoms of Dry Eye Disease — Stopped early
• A Clinical Trial on Safety and Efficacy of CBT-001 in Patients With Pterygium — Running, not enrolling
• Evaluate the TetraLens, a Tetracaine Releasing Therapeutic Bandage Contact Lens in Patients Undergoing PRK Procedure — Completed
• In Clinic Optometrist Insertion of Dextenza Prior to Cataract Surgery — Completed
• Clinical Investigation of the Next-Generation Intraocular Lens — Completed
• Next Generation Cataract Surgery Study — Completed
• User Acceptability Evaluation of Pseudophakic Patients Previously Implanted With the TECNIS Odyssey IOL — Completed
• Study to Evaluate the Efficacy and Safety of Intravitreal OTX-TKI (Ocular Therapeutix) (Axitinib Implant) in Subjects With Neovascular Age-Related Macular Degeneration — Running, not enrolling
• A Study to Evaluate Safety and Tolerability of QLS-101 in NTG — Completed
• Randomized Study Comparing Two Models of a Travoprost Intraocular Implant to Timolol Maleate Ophthalmic Solution, 0.5% — Completed
• Artisan Aphakia Lens for the Correction of Aphakia (Secondary) in Adults — Paused
• The RESTORE Study, A Randomized, Controlled, Masked (Reading Center) Prospective Study — Completed
• Clinical Outcomes of Patients Implanted With the RxSight Light Adjustable Lens (LAL) — Withdrawn before enrolling
• Effect of Negative Pressure on Pattern Electroretinography Readings — Withdrawn before enrolling
• Vivity Outcomes in Patients With Early Stage Glaucoma — Completed
• Binocular Custom Vision Utilizing The Light Adjustable Lens (LAL) — Completed
• Post-approval Follow-up Study of the IC-8 Apthera Intraocular Lens (IOL) — Completed
• Study of Exchange of Travoprost Intraocular Implant — Completed
• Post-Approval Study of the TECNIS SYMFONY® Toric Lenses — Completed
• Long Term Outcomes of Vivity Intra Ocular Lens(IOL) Versus Control — Completed
• Negative Pressure Applied by the Equinox MPD for Severe Open Angle Glaucoma — Completed
• Clinical Evaluation of a Small Aperture Extended Depth of Focus Intraocular Lens — Completed
• An Observational, Qualitative Study Assessing Eye Drop Administration — Status unconfirmed
• A Phase 2 Study Evaluating the Safety and Efficacy of Netarsudil Ophthalmic Solution in Patients With Corneal Edema Due to Fuchs Corneal Dystrophy — Completed
• Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in Participants With Presbyopia — Completed
• Clinical Investigation of the Safety and Effectiveness of an Investigational Model of the TECNIS® Intraocular Lens — Completed
• Safety and Efficacy of Corneal Collagen Cross-Linking in Eyes With Keratoconus — Stopped early
• Safety and Efficacy of Corneal Collagen Cross-linking Following LASIK for Treatment of Hyperopia and Hyperopic Astigmatism — Stopped early
• Safety and Efficacy Study of Corneal Collagen Cross-Linking in Eyes With Keratoconus — Completed
• Analysis of Defocus Curve of Pre-Presbyopic and Emerging Presbyopic Patients — Completed
• Correction of Myopia Wtih or Without Astigmatism Using the VisuMax™ Femtosecond Laser — Completed
• Ocular Surface Disease Changes After iStent or iStent Inject Implantation With Phacoemulsification — Completed
• Post-Approval Study of the Tecnis® Toric IOL — Completed
• Ocular Bandage Gel (OBG) Pivotal Trial in Patients Undergoing Photorefractive Keratectomy ("PRK") — Completed