Casey Eye Institute - Oregon Health & Science University
Portland, Oregon, 97239, United States
NCT Number: NCT07174401
The main purpose of this study is to learn more about how Rocklatan eye drops affects blood flow in the eye. The secondary purpose is to see if our study devices can detect changes in blood flow before and after instillation of Rocklatan.
Trial opening soon.
Get Notified21 year and older
All sexes
Interventional
Phase 4
Portland, Oregon, 97239, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The eye not selected as the study eye will be used for comparison so both eyes will be imaged with the study devices to assess blood flow changes.
One OCT device is FDA-cleared while the other is still experimental. Both devices assess blood flow in different ways.
Time frame: From enrollment to end of treatment at 11-12 months
The primary outcome measure will be change in the overall peripapillary NFLP CD measured at 6 months and 11-12 month endpoint visits compared to baseline values.
Time frame: From enrollment to end of treatment at 11-12 months
Secondary outcome measures will include change in the TRBF measured at 6 months or 11-12 month endpoint visits compared to baseline.
Trial opening soon.
Get NotifiedOregon Health and Science University
Other
Rocklatan Trial With Optical Coherence Tomography Study of Retinal Perfusion
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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