Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05885022

Feasibility Clinical Evaluation of the Calibreye System

Led by Myra Vision Inc. · Updated on 2025-12-15

60

Participants Needed

4

Research Sites

287 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To evaluate the safety and feasibility of the Calibreye System in patients with open angle glaucoma.

CONDITIONS

Official Title

Feasibility Clinical Evaluation of the Calibreye System

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Open angle, pseudoexfoliative or pigmentary glaucoma
  • Intraocular pressure at preoperative visit of 65 18mmHg and 64 45mmHg
  • Visual field mean deviation score of -3dB or worse
  • Area of healthy, free and mobile conjunctiva in the target quadrant
  • Shaffer angle grade 65 3 in the target quadrant
Not Eligible

You will not qualify if you...

  • Angle closure glaucoma
  • Congenital, neovascular or other secondary glaucomas
  • Previous intraocular surgery except laser trabeculoplasty or uncomplicated phacoemulsification with IOL more than 3 months prior
  • Previous glaucoma shunt or valve in the target quadrant
  • Clinically significant inflammation or infection in the study eye within 30 days before preoperative visit
  • History of corneal surgery, corneal opacities, or corneal disease
  • Active diabetic retinopathy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Dr. Agarwal's Eye Hospital Ltd.

Chennai, India, 600018

Active, Not Recruiting

2

Centro Oftalmologico de Chihuahua

Chihuahua City, Mexico

Actively Recruiting

3

Oftalmología Láser de Puebla S.C.

Puebla City, Mexico, 72540

Actively Recruiting

4

Panama Eye Center

Panama City, Panama

Actively Recruiting

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Research Team

S

Shienal Patel

CONTACT

M

Michelle Tran

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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