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Comparing NGENUITY vs Conventional Microscope in a New Hydrus User

NCT05529966 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2025-04-17

Study results available
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Summary

To compare the potential efficiency and educational value of using NGENUITY (3D camera system, FDA approved for this indication) vs the conventional microscope for Hydrus microstent placement by new users.

Conditions

Interventions

DEVICE

NGENUITY

Device for 3-D viewing during placement of micro-stent placement.

DEVICE

Conventional microscope

Device for stereoscopic viewing during placement of micro-stent placement.

Sponsors & Collaborators

Principal Investigators

  • Robert T Chang, MD · Stanford University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-13
Primary Completion
2024-03-22
Completion
2024-03-22
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05529966 on ClinicalTrials.gov