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NCT05729477 · ClinicalTrials.gov registry record · NA

A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device

A NA study, sponsored by Carl Zeiss Meditec.

Terminated
Registry status
NA
Development phase
402
Enrollment target

NCT05729477 is a NA study that was terminated before completion, run by Carl Zeiss Meditec. The registered enrollment target is 402 participants.

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The verdict

NCT05729477, a NA study, was terminated before completion, sponsored by Carl Zeiss Meditec.

TERMINATED
Registry status
NA
Development phase
402 participants
Enrollment target

Study Summary

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.

Interventions

  • DEVICE miCOR System
  • DEVICE Phaco Subject Cohort

Trial Details

FieldValue
Enrollment Target 402 participants
Start Date 2022-12-06
Est. Completion 2025-12-30
Phase NA

Sponsor

Carl Zeiss Meditec

18 total trials

What the Registry Record Tells You About NCT05729477

The ClinicalTrials.gov registry entry for NCT05729477 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 402 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Carl Zeiss Meditec, which has 18 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which miCOR System is the first listed.

NCT05729477 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05729477 about?

NCT05729477 is a clinical study titled "A Prospective Multicenter Study To Assess The Clinical Outcomes Of Current Phacoemulsification Approach To Cataract Extraction Versus The Micor System Device". 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/aspir...

What is the current status of trial NCT05729477?

This trial is currently terminated. It is a NA study. The enrollment target is 402 participants. The study started on 2022-12-06. Estimated completion is 2025-12-30.

What interventions are being tested in trial NCT05729477?

The interventions under investigation include: miCOR System (DEVICE), Phaco Subject Cohort (DEVICE).

Who is sponsoring clinical trial NCT05729477?

This trial is sponsored by Carl Zeiss Meditec, which has 18 total clinical trials registered on ClinicalTrials.gov.

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 mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.