Carl Zeiss Meditec ((GB:0DHC)) announced an update on their ongoing clinical study.
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The clinical study titled ‘A Prospective, Randomized, Controlled, Observer-masked, Multi-center Clinical Trial to Demonstrate the Safety and Effectiveness of the Extended Depth of Focus AT LARA 829MP Posterior Chamber Intraocular Lens for Correction of Aphakia’ aims to evaluate the safety and effectiveness of the Extended Depth of Focus (EDF) intraocular lens compared to a Monofocal intraocular lens. This study is significant as it addresses the treatment of cataract senile, a common condition affecting vision in older adults.
The intervention being tested involves two types of intraocular lenses: the Extended Depth of Focus (EDF) lens and the Monofocal lens. The EDF lens is designed to provide a broader range of clear vision, potentially reducing the need for glasses after cataract surgery.
This study is designed as a randomized, controlled trial with a parallel intervention model. It employs double masking, meaning both participants and investigators are unaware of which lens is being used, to ensure unbiased results. The primary purpose of the study is treatment-focused.
The study is set to begin recruiting participants on July 11, 2025, with the last update submitted on July 21, 2025. These dates are crucial as they mark the initiation of the study and the most recent updates, indicating the study’s progress and timeline.
The outcome of this study could have significant market implications for Carl Zeiss Meditec AG, potentially boosting its stock performance and investor confidence if the EDF lens proves to be more effective. This could also impact competitors in the ophthalmic device industry, prompting advancements in lens technology.
The study is currently not yet recruiting, with further details available on the ClinicalTrials portal.