MedTrace Logo

Comparison of Silicone and Porous Plate Ahmed Glaucoma Valves

NCT01883856 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2020-10-19

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate and compare the clinical outcomes after implantation of the porous plate (polyethylene) (Model M4) Ahmed Glaucoma Valve with the silicone plate Ahmed Glaucoma Valve (Model FP7) in participants with refractory glaucoma.

Conditions

Interventions

DEVICE

Silicone plate Ahmed Glaucoma Valve (Model FP7)

This intervention is conducted as a surgical intervention.

DEVICE

Porous Plate Ahmed Glaucoma Valve (Model M4)

This intervention is conducted as a surgical intervention.

Sponsors & Collaborators

  • New World Medical, Inc.

    collaborator INDUSTRY

  • Peter Netland, MD

    lead OTHER

Principal Investigators

  • Peter A Netland, MD, PhD · University of Virginia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2017-09-10
Completion
2018-08-27

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT01883856 on ClinicalTrials.gov