RecruitingNCT06577857

Inferonasal MIMS® Procedure: Long-Term Follow-Up Extension Study

Minimally Invasive Micro Sclerostomy (MIMS®) Inferonasal Procedure: Long-Term Follow-Up Extension Study


Sponsor

Sanoculis Ltd

Enrollment

53 participants

Start Date

Nov 4, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

A long-term (24 and 30 months) follow-up extension, prospective, non-interventional, open label study for data collection from subjects who underwent prior MIMS® inferonasal surgery, in continuation of the previous clinical investigation with the MIMS® Device (MMS-EEU-5).


Eligibility

Min Age: 40 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This study is a long-term follow-up extension for people who previously had the MIMS glaucoma procedure performed in the lower part of the eye (inferonasal region). The goal is to track how well the procedure continues to work over many years in reducing eye pressure. **You may be eligible if...** - You previously had the inferonasal MIMS procedure - Your surgery was performed at least 24 months before you enroll in this extension study **You may NOT be eligible if...** - You did not previously have the MIMS inferonasal procedure - Your surgery was performed less than 24 months ago Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEInferonasal Minimally Invasive Micro Sclerostomy

The Inferonasal MIMS® procedure uses the proprietary MIMS® device, which creates a sclerostomy in the inferonasal quadrant of the eye.


Locations(1)

S. Malayan Eye Center

Yerevan, Armenia

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NCT06577857


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