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Recruiting NCT06953349

NCT06953349 Efficacy of Surgical Systems in Combination With Phacoemulsification: a Retrospective Analysis

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Clinical Trial Summary
NCT ID NCT06953349
Status Recruiting
Phase
Sponsor Barnet Dulaney Perkins Eye Centers
Condition Open-Angle Glaucoma
Study Type OBSERVATIONAL
Enrollment 300 participants
Start Date 2025-03-31
Primary Completion 2025-11-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Real-World efficacy of Hydrus Microstent with OMNI Surgical System in combination with Phacoemulsification: a retrospective analysis

Eligibility Fast-Check

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

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 300 participants in total. It began in 2025-03-31 with a primary completion date of 2025-11-30.

⚠ 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

Real-World efficacy of Hydrus Microstent with OMNI Surgical System in combination with Phacoemulsification: a retrospective analysis

Eligibility Criteria

Inclusion Criteria: * Subjects with h/o CEIOL/OMNI/Hydrus (chosen based on subjects on more than 1 medication pre-operatively) with at least 3 years of follow up data * have Glaucoma Exclusion Criteria: * Patients with angle closure glaucoma or secondary forms of glaucoma due to neovascularization of the angle, uveitic glaucoma, congenital glaucoma, or glaucoma due to congenital anomalies. * Patients with refractory CME or CME persisting 3 months or more post-operatively * Patients with incomplete IOP, medication logs or VF data within post-operative period * Prior incisional surgery or MIGS

Contact & Investigator

Central Contact

Derek J Arnson, Master of Education

✉ derek.arnson@researchavp.com

📞 4804201005

Principal Investigator

Christine Funke, Medical Doctor

PRINCIPAL INVESTIGATOR

Barnet Dulaney Perkins Eye Centers

Frequently Asked Questions

Who can join the NCT06953349 clinical trial?

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

Is NCT06953349 currently recruiting?

Yes, NCT06953349 is actively recruiting participants. Contact the research team at derek.arnson@researchavp.com for enrollment information.

Where is the NCT06953349 trial being conducted?

This trial is being conducted at Mesa, United States.

Who is sponsoring the NCT06953349 clinical trial?

NCT06953349 is sponsored by Barnet Dulaney Perkins Eye Centers. The principal investigator is Christine Funke, Medical Doctor at Barnet Dulaney Perkins Eye Centers. The trial plans to enroll 300 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology