An Observational, Qualitative Study Assessing Eye Drop Administration
Status unconfirmed
Conditions studied: Ocular Injury
In brief
This is a prospective, observational, consecutive, qualitative, multicenter study. Based on the available published evidence that supports patient challenges with eyedrop administration, the purpose of this video-capture study is to evaluate a more real-world population of consenting patients, regardless of age, with or without visual impairment, at routine eyecare visits. To date, no studies have been performed evaluating a real-world population consisting of daily routine eyecare clinic patients with or without visual impairment. This study will help to determine the ability to achieve success with self-administration of eyedrops in the real world.
Key facts
- Study ID
- NCT05307081
- Run by
- Ocular Therapeutix, Inc.
- People needed
- 300
- Starts
- 2022-04-21
- Expected to finish
- 2023-12-01
- Last updated by the study team
- 2022-09-16
Who can join
Age: any. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients or parents of minor patients who consent to participating in the study
You may not qualify if…
- Any patient who does not consent to study participation
Where it is running
- Vance Thompson Vision — Sioux Falls, South Dakota, United States (enrolling)
Full record on ClinicalTrials.gov
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