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NCT07816692Recruiting

iDose TR Administration in an Office-Based Surgery Setting

Real-World Evidence Observational Study to Evaluate the Safety of iDose® TR (Travoprost Intracameral Implant) 75 µg in an Office-Based Surgery Setting

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
8 Sept 2026
Start date
13 May 2026
Primary completion date
Mar 2027
Lead sponsor
Glaukos Corporation
NCT number
NCT07816692

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 13 May 2026 to the primary completion date, Mar 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior administration of iDose TR or administration of an investigational intracameral implant in the study eye
  • Recent ocular surgery

Other illness

  • Active ocular infection or inflammation
  • History of hypersensitivity to travoprost or implant components
  • Uncontrolled systemic disease
  • Any condition preventing safe implantation

Who the study is looking for

  • Diagnosis of Open angle glaucoma (OAG) or ocular hypertension (OHT)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
AustinUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.