Ireland
--:--IST
Recruiting Observational

iDose TR Administration in an Office-Based Surgery Setting

NCT07816692 · tracked via the Priya Life Science USA tracker
Phase
Observational
Started
2026-05-13
Last updated
2026-09-30

Condition(s) studied

Open Angle Glaucoma (OAG)Ocular Hypertension (OHT)

Investigational drug(s) / intervention(s)

iDose TR (travoprost intracameral implant) 75 µg

iDose TR (travoprost intracameral implant) 75 µg: Travoprost-releasing implant preloaded in a sterile, single-use inserter.

Study summary

Clinical in-use observational trial to evaluate the administration of iDose TR (travoprost intracameral implant) in an office-based surgery setting.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of Open angle glaucoma (OAG) or ocular hypertension (OHT) Exclusion Criteria: * Prior administration of iDose TR or administration of an investigational intracameral implant in the study eye * Active ocular infection or inflammation * History of hypersensitivity to travoprost or implant components * Recent ocular surgery * Uncontrolled systemic disease * Any condition preventing safe implantation

Primary outcome measure(s)

  • Successful administration of iDose TR in an office-based surgical setting. — 3 months
    Number of subjects that received iDose TR in an office-based surgical setting by the Investigator.

Trial sites (1)

FacilityCityRegionStatus
Glaukos Investigative Site Austin Texas Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07816692 on ClinicalTrials.gov ↗ ← All trials in the USA