Clinical Trials in the USA / NCT07816692
Recruiting
Observational
iDose TR Administration in an Office-Based Surgery Setting
NCT07816692 · tracked via the Priya Life Science USA tracker
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Glaukos Investigative Site | Austin | Texas | Recruiting |
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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