Eyedrop lifts droopy eyelids after facial paralysis?
NCT ID NCT05945615
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested an FDA-approved eyedrop (oxymetazoline 0.1%) in 36 adults with eyelid droop caused by facial nerve miswiring after paralysis. The goal was to see if the drop could temporarily raise the eyelid, improve vision, and reduce abnormal muscle spasms. Researchers measured changes in eyelid position, facial function, and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Oxymetazoline 0.1% ophthalmic solution (Upneeq)
- What this could lead to
- If it works, this could offer a simple eyedrop treatment to temporarily lift the eyelid and improve vision and appearance in people with eyelid droop after facial paralysis.
- What could go wrong
- This is a small, completed trial with only 36 participants. The medication is already FDA-approved for other causes of eyelid droop, but its effect on droop due to nerve miswiring may be limited or not last long.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
36 people
The number who actually took part.
- Started
-
Jan 2024
- Finished
-
Jan 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 99 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Over 18 years of age 2. Primary diagnosis of nonflaccid facial paralysis (aberrant regeneration syndrome) and acquired blepharoptosis. Exclusion Criteria: 1. Patients under the age of 18 2. Patients on cardiac glycosides 3. Patients on MAO inhibitors 4. Patients with angle closure glaucoma 5. Patients who experience asymmetrical eye opening due to weakness (e.g. lagophthalmos).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
M.S. Hershey Medical Center
Hershey, Pennsylvania, 17033, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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