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Study identifier: NCT07235592 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

PRESERFLO™ MicroShunt XI Observational PMCF Study With no Control Group

Condition: Primary Open Angle Glaucoma  ·  Sponsor: Santen SAS

PhaseN/A
Planned participants112
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNo

About this study

The purpose of this study is to collect safety and performance data on the PRESERFLO™ MicroShunt XI in patients diagnosed with primary open angle glaucoma who are inadequately controlled on maximum tolerated medical therapy with intraocular pressure ≥18 mmHg and ≤35 mmHg and/or where glaucoma progression warrants surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Study Director / Medical Monitor Raymund Angeles  ·  510-368-9861  ·  raymund.angeles@santen.com

Santen SAS Clinical Operations  ·  bianca.groenendijk@santen.com

Always discuss trial participation with your own doctor first.

Locations (11)

AKH WienVienna, AustriaRecruiting
Glaucoma Clinic, UZ LeuvenLeuven, BelgiumRecruiting
Internationale Innovative Opthalmochirurgie GbRDüsseldorf, GermanyRecruiting
Universitätsklinikum Tübingen, Department für AugenheilkundeTübingen, GermanyNot Yet Recruiting
Irccs Fondazione G. B. BiettiRome, ItalyRecruiting
Policlinico Universitario MolinetteTurin, ItalyNot Yet Recruiting
Universiteitskliniek voor Oogheelkunde MaastrichtMaastricht, NetherlandsNot Yet Recruiting
ULS Santa Maria, LisboaLisbon, PortugalNot Yet Recruiting
Hospital Clinico San CarlosSan Carlos, SpainNot Yet Recruiting
Guy's and St. Thomas' NHS Foundation TrustLondon, United KingdomRecruiting
Moorfields Eye Hospital NHS Foundation TrustLondon, United KingdomNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07235592