A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device
Stopped early · Not applicable
Conditions studied: Cataract Surgery
In brief
The purpose of this research study is to evaluate the clinical outcomes of current phacoemulsification approaches to cataract extraction involving high-frequency thermogenic energy versus the use of the MICOR System device using low-energy segment removal with a micro-interventional irrigation/aspiration port to evacuate the lens in subjects undergoing routine cataract surgery.
Key facts
- Study ID
- NCT05729477
- Run by
- Carl Zeiss Meditec, Inc.
- People needed
- 402
- Starts
- 2022-12-06
- Expected to finish
- 2025-12-30
- Last updated by the study team
- 2026-05-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Able to understand study requirements, willing to follow study instructions and willing to return for required study follow-up visits.
- Willing and able to understand and complete the informed consent document.
- Subjects with a cataract grade of 1 to 4+ and are scheduled to undergo cataract surgery.
- Subjects ≥ 18 years of age.
You may not qualify if…
- Subjects, who in the opinion of the investigator, have "compromised" eye(s); no comorbidities and no patients undergoing concurrent corneal surgery with cataract extraction.
- Concurrent participation or participation in any clinical trial up to 30 days prior to preoperative visit.
- Subjects that are pregnant, lactating or planning to become pregnant during the course of the study.
Where it is running
- Argus Research at Cape Coral Eye Center — Cape Coral, Florida, United States
- Mittleman Eye — West Palm Beach, Florida, United States
- Wolfe Eye Clinic — Hiawatha, Iowa, United States
- Penn State Health Eye Center — Hershey, Pennsylvania, United States
- Virginia Eye Consultants — Norfolk, Virginia, United States
- The eye Centers of Racine and Kenosh — Racine, Wisconsin, United States
Full record on ClinicalTrials.gov
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