Phase 4 IOP Signals Associated With ILUVIEN®
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Ocular |
| Therapuetic Areas: | Ophthalmology |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 1/25/2019 |
| Start Date: | May 6, 2015 |
| End Date: | January 2020 |
A Phase 4 Safety Study of IOP Signals in Patients Treated With ILUVIEN® (Fluocinolone Acetonide Intravitreal Implant) 0.19 mg
This study will assess the safety in patients treated with ILUVIEN, with primary focus on
IOP.
IOP.
The specific objectives include the study of intraocular pressure (IOP) related data in
patients who received ILUVIEN and how it relates to the patient's experiences following prior
treatment with a course of corticosteroid which did not result in a clinically significant
IOP elevation.
patients who received ILUVIEN and how it relates to the patient's experiences following prior
treatment with a course of corticosteroid which did not result in a clinically significant
IOP elevation.
Inclusion Criteria:
- Patients who are eligible for treatment with ILUVIEN based on the Prescribing
Information.
Exclusion Criteria:
- Patients who are unable to understand and sign the Informed Consent Form.
We found this trial at
41
sites
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Wayne State University Founded in 1868, Wayne State University is a nationally recognized metropolitan research...
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Johns Hopkins Hospital Patients are the focus of everything we do at The Johns Hopkins...
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University of Illinois at Chicago A major research university in the heart of one of...
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