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NCT07220876 · ClinicalTrials.gov registry record · NA

Safety and Effectiveness of the VisiPlate Aqueous Shunt in Patients With Refractory Open-Angle Glaucoma

A NA study of Open Angle Glaucoma (OAG), sponsored by Avisi Technologies.

Recruiting
Registry status
NA
Development phase
165
Enrollment target
12
Study locations

NCT07220876: Recruiting NA study of Open Angle Glaucoma (OAG), sponsored by Avisi Technologies.

NCT07220876 is a NA study of Open Angle Glaucoma (OAG) that is actively recruiting participants, run by Avisi Technologies. The registered enrollment target is 165 participants, above the 35-participant average among 5 other Open Angle Glaucoma (OAG) trials with a reported enrollment target (371% higher). The trial reports 12 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07220876, a NA study of Open Angle Glaucoma (OAG), is actively recruiting participants, sponsored by Avisi Technologies.

RECRUITING
Registry status
NA
Development phase
165 participants
Enrollment target
12
Study locations

Study Summary

A Prospective, Multicenter, Single-Arm, Open-Label Clinical Trial

Primary Outcome

The eye is filled with a special fluid. The intraocular pressure is the amount of fluid that builds up in the eye. The primary outcome is the number of people whose eye pressure went down by at least 20%.

Conditions Studied

Interventions

  • DEVICE VisiPlate Glaucoma Implant

Study Locations (12)

Colorado

  • ICON Eye Care - Grand Junction
  • Mile High Eye Institute - Sheridan

Pennsylvania

  • Scheie Eye Institute - Philadelphia
  • Wills Eye Hospital - Philadelphia

Texas

  • Glaucoma Associates of Texas - Dallas
  • University of Texas Southwestern - Dallas

Other

  • Lynette Venter - Bloemfontein
  • Pretoria Eye Institute - Pretoria

Arizona

  • Arizona Advanced Eye Research - Glendale

California

  • Sacramento Eye Consultants - Sacramento

Ohio

  • Cleveland Clinic- Cole Eye Institute - Cleveland

Wisconsin

  • The Eye Centers of Racine & Kenosha - Kenosha

Trial Details

FieldValue
Enrollment Target 165 participants
Start Date 2025-11-07
Est. Completion 2027-10
Phase NA
Avisi Technologies

1 total trials

What NCT07220876 shows while recruiting

NCT07220876 is an interventional study that assigns participants to a tested intervention. The registered 165 participants enrollment target is mid-sized for trials with a published cap, above the 35-participant average among 5 other Open Angle Glaucoma (OAG) trials with a reported enrollment target (371% higher).

The record links to 1 condition, with Open Angle Glaucoma (OAG) appearing as the primary indexed condition, and to 1 intervention - of which VisiPlate Glaucoma Implant is the first listed.

NCT07220876 lists 12 locations in 8 states (Colorado, Pennsylvania, Texas).

Frequently Asked Questions

What is clinical trial NCT07220876 about?

NCT07220876 is a clinical study titled "Safety and Effectiveness of the VisiPlate Aqueous Shunt in Patients With Refractory Open-Angle Glaucoma". A Prospective, Multicenter, Single-Arm, Open-Label Clinical Trial

What is the current status of trial NCT07220876?

This trial is currently recruiting. It is a NA study. The enrollment target is 165 participants. The study started on 2025-11-07. Estimated completion is 2027-10.

What conditions does trial NCT07220876 study?

This clinical trial studies the following conditions: Open Angle Glaucoma (OAG).

What interventions are being tested in trial NCT07220876?

The interventions under investigation include: VisiPlate Glaucoma Implant (DEVICE).

Who is sponsoring clinical trial NCT07220876?

This trial is sponsored by Avisi Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07220876 being conducted?

This trial has 12 study locations across Arizona, California, Colorado, Ohio, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Open Angle Glaucoma (OAG)

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT07220876, the US trial registry maintained by the National Library of Medicine. NCT07220876 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.