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Recruiting NCT05885022

NCT05885022 Feasibility Clinical Evaluation of the Calibreye System

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Clinical Trial Summary
NCT ID NCT05885022
Status Recruiting
Phase
Sponsor Myra Vision Inc.
Condition Glaucoma, Open-Angle
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2023-05-31
Primary Completion 2027-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Calibreye System

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2023-05-31 with a primary completion date of 2027-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Eligibility Criteria

Inclusion Criteria: * Open angle, pseudoexfoliative or pigmentary glaucoma * IOP at preoperative visit of ≥ 18mmHg and ≤ 45mmHg * Visual field mean deviation score of -3dB or worse * Area of healthy, free and mobile conjunctiva in the target quadrant * Shaffer angle grade ≥ 3 in the target quadrant Exclusion Criteria: * Angle closure glaucoma * Congenital, neovascular or other secondary glaucomas * Previous intraocular surgery (with the exception of laser trabeculoplasty or uncomplicated phacoemulsification with IOL occurring \> 3 months prior to the preoperative visit) * Previous glaucoma shunt/valve in the target quadrant * Clinically significant inflammation or infection in the study eye within 30 days prior to the preoperative visit * History of corneal surgery, corneal opacities or corneal disease * Active diabetic retinopathy

Contact & Investigator

Central Contact

Shienal Patel

✉ info@myravision.com

📞 14085602500

Principal Investigator

Keith Barton, MD

STUDY CHAIR

Moorfields Eye Hospital NHS Foundation Trust

Frequently Asked Questions

Who can join the NCT05885022 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Glaucoma, Open-Angle. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05885022 currently recruiting?

Yes, NCT05885022 is actively recruiting participants. Contact the research team at info@myravision.com for enrollment information.

Where is the NCT05885022 trial being conducted?

This trial is being conducted at Chennai, India, Chihuahua City, Mexico, Puebla City, Mexico, Panama City, Panama.

Who is sponsoring the NCT05885022 clinical trial?

NCT05885022 is sponsored by Myra Vision Inc.. The principal investigator is Keith Barton, MD at Moorfields Eye Hospital NHS Foundation Trust. The trial plans to enroll 60 participants.

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