Clinical Trials Directory

Trials / Completed

CompletedNCT07051174

The Minimally Invasive Micro Sclerostomy (MIMS®) System is Intended for the Reduction of Elevated Intraocular Pressure (IOP): The Minimally Invasive Micro Sclerostomy (MIMS®) System is Intended for the Reduction of Elevated Intraocular Pressure (IOP)

Minimally Invasive Micro Sclerostomy System - Long- Term Follow-Up Extension Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Sanoculis Ltd · Industry
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

No new investigational device is used in this study. This study is an extension follow up study conducted in continuation of the prior MIMS® study (see: STUDY ID: MMS EEU-1), in which the long-term (i.e., 28, 36, 42 months) clinical outcomes of Minimally Invasive Micro Sclerostomy System \[MIMS® System\] \[CE Marked device\] are evaluated.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTMIMSThis study is an extension follow up study conducted in continuation of the prior MIMS® study (see: STUDY ID: MMS EEU-1), in which the long-term (i.e., 28, 36, 42 months) clinical outcomes of Minimally Invasive Micro Sclerostomy System \[MIMS® System\] \[CE Marked device\] are evaluated.

Timeline

Start date
2022-04-11
Primary completion
2023-08-30
Completion
2023-10-27
First posted
2025-07-04
Last updated
2025-07-04

Locations

1 site across 1 country: Armenia

Source: ClinicalTrials.gov record NCT07051174. Inclusion in this directory is not an endorsement.