Iridex Announces the Publication of Two-Year Independent Study Supporting Benefits of MicroPulse® Technology for Early to Advanced Glaucoma
The retrospective study reported sustained pressure reductions and lower medication use over 24 months.
Sentiment and the balance of points
Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.
Rhea-AI Summary
Iridex (IRIX) announced publication of a two-year study evaluating MicroPulse laser therapy in patients with early, moderate and advanced glaucoma. The retrospective study, published in the International Journal of Ophthalmology, evaluated 84 eyes of 53 patients with primary open-angle or primary angle-closure glaucoma.
At 24 months, mean intraocular pressure decreased from 22.32 to 14.05 mmHg, and mean topical pressure-lowering medication use fell from 2.96 to 2.38. Treatment success rates were 86% for open-angle glaucoma and 81% for angle-closure glaucoma. No complications or reductions in visual acuity were reported, and visual field measurements remained stable. All patients previously taking oral acetazolamide discontinued it, with none restarting during follow-up.
Positive
- Minor pointMean intraocular pressure fell from 22.32 to 14.05 mmHg, with reductions sustained over two years.
- Minor pointMean topical pressure-lowering medication use decreased from 2.96 to 2.38 at 24 months.
- Minor pointTreatment success at 24 months reached 86% in open-angle and 81% in angle-closure glaucoma eyes.
- Minor pointNo complications or reductions in visual acuity were reported during follow-up.
- Minor pointOral acetazolamide was discontinued by all patients previously receiving it, with none restarting over two years.
- Minor pointVisual field measurements remained stable during follow-up in both glaucoma groups.
Negative
- Minor pointEvidence came from a retrospective study of 84 eyes in 53 patients.
- Minor pointStudy eligibility excluded patients with prior incisional glaucoma surgery.
Key Figures
- Study population
- 84 eyes; 53 patients
- Retrospective study
- Follow-up duration
- 24 months
- Clinical study
- Mean intraocular pressure
- 22.32 mmHg at baseline to 14.05 mmHg
- Reduction sustained throughout follow-up
- Mean topical IOP-lowering medications
- 2.96 at baseline to 2.38
- At 24 months
- Treatment success
- 86% in POAG eyes; 81% in PACG eyes
- At 24 months
- Reported complications or visual acuity reductions
- None reported
- During follow-up
Key Terms
transscleral laser therapy medical
intraocular pressure medical
primary open-angle glaucoma medical
primary angle-closure glaucoma medical
selective laser trabeculoplasty medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
Study reports sustained IOP reduction and reduced medication burden over 24 months
SAN JOSE, Calif., Oct. 12, 2026 (GLOBE NEWSWIRE) -- Iridex Corporation (Nasdaq: IRIX), a worldwide leader in innovative laser-based medical systems, delivery devices, and accessories for the treatment of glaucoma and retinal diseases, today announced the publication of a two-year clinical study demonstrating favorable outcomes with transscleral laser therapy (TLT) using MicroPulse® Technology (referred to as MicroPulse TLT) in patients with early, moderate, and advanced primary glaucoma.
“These two-year results are particularly meaningful because they show sustained IOP reduction and reduced medication burden in patients with early-stage glaucoma, as well as in those with moderate and advanced disease,” said Michele Lanza, MD, lead author of the study. “The findings suggest that MicroPulse TLT may have a role earlier in the glaucoma treatment continuum than has traditionally been considered.”
Published in the International Journal of Ophthalmology, the retrospective study evaluated 84 eyes of 53 patients with primary open-angle glaucoma (POAG) or primary angle-closure glaucoma (PACG). Led by Dr. Lanza of the Università della Campania Luigi Vanvitelli in Naples, Italy, the study used the Iridex Cyclo G6® Laser with the original MicroPulse® P3 Delivery Device. Patients with prior incisional glaucoma surgery were excluded, while those who had undergone selective laser trabeculoplasty (SLT) more than three years earlier remained eligible for inclusion.
“We are encouraged by the sustained outcomes reported in this study and the growing body of clinical evidence supporting MicroPulse TLT,” said Patrick Mercer, President and Chief Executive Officer of Iridex. “These findings further reinforce our commitment to advancing laser-based treatment options for patients with glaucoma.”
Key Findings at 24 Months
- Mean intraocular pressure (IOP) decreased significantly from 22.32 mmHg at baseline to 14.05 mmHg, with reductions sustained throughout the two-year follow-up
- Mean number of topical IOP-lowering medications decreased from 2.96 at baseline to 2.38
- Treatment success rates were
86% in POAG eyes and81% in PACG eyes - No complications or reductions in visual acuity were reported during follow-up
Additional findings included the discontinuation of oral acetazolamide among all patients receiving the medication before MicroPulse TLT, with none requiring reinitiation during the two-year follow-up period. Further, visual field measurements remained stable during follow-up in both the POAG and PACG groups.
About the Study
Lanza M, Fattore I, Ambrosio S, Abbate F, Boccia R, Serra L, Cangiano T, Simonelli F. Safety and efficacy of micropulse transscleral laser therapy for glaucoma: a two-year follow-up. International Journal of Ophthalmology. 2026;19(9):1731-1738. doi:10.18240/ijo.2026.09.08.
About Iridex Corporation
Iridex Corporation is a worldwide leader in developing, manufacturing, and marketing innovative and versatile laser-based medical systems, which include capital equipment and consumable probes for the ophthalmology market. The Company’s proprietary MicroPulse® technology delivers the therapeutic benefits of laser treatment while minimizing tissue damage, offering a safe, effective, and proven treatment for targeted sight-threatening eye conditions. Iridex’s current product line is used for the treatment of glaucoma and diabetic macular edema (DME) and other retinal diseases. Iridex products are sold in the United States through a direct sales force and internationally primarily through a network of independent distributors into more than 100 countries.
For additional information, visit www.iridex.com.
Investor Relations Contact
Philip Taylor
Gilmartin Group
investors@iridex.com
Media Contact
Joan Stauffer
jstauffer@iridex.com
Iridex, the Iridex logo, MicroPulse, the MicroPulse logo, Cyclo G6, and MicroPulse P3 are registered trademarks of Iridex.
FAQ
AI-generated questions and answers. How Rhea-AI works. Not financial advice.
What did Iridex's two-year MicroPulse glaucoma study show?
At 24 months, mean intraocular pressure fell from 22.32 to 14.05 mmHg, while mean topical pressure-lowering medication use decreased from 2.96 to 2.38. Treatment success rates were 86% in primary open-angle glaucoma eyes and 81% in primary angle-closure glaucoma eyes.
Were patients with previous glaucoma procedures included in the Iridex MicroPulse study?
Patients with prior incisional glaucoma surgery were excluded, but patients who had undergone selective laser trabeculoplasty more than three years earlier remained eligible for inclusion.