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CompletedNCT05945615Updated Mar 9, 2026

Oxymetazoline Drops for Acquired Blepharoptosis From Synkinesis

A Phase 3 interventional study of Oxymetazoline 0.1% (Pf) Oph Soln Ud and Preservative free lubricating drops in Blepharoptosis, Synkinesis and Hyperkinesis, sponsored by Milton S. Hershey Medical Center. Completed at 1 site in United States. Open to participants aged 18 Years to 99 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-09.

Sponsored by Milton S. Hershey Medical Center · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
18 Years to 99 Years
Sex
All
01

Study summary

After an episode of facial paralysis, as nerves recover, they aberrantly regenerate and send additional branches to the incorrect muscles in addition to the intended muscle. This leads to what is known as Aberrant Regeneration Syndrome, Post-paralysis Synkinesis, or Nonflaccid Facial Paralysis. It is characterized by poor facial symmetry and function, hypertonic facial muscles at rest, and abnormal facial movements. One sequela is acquired blepharoptosis causing a smaller ocular aperture, visual field obstruction, cosmetic deformity, and abnormal periocular spasms. This study aims to evaluate an FDA approved medication for acquired blepharoptosis due to synkinesis/hyperkinesis as an adjunct to treatment.

Read the detailed description

Broadly, synkinesis is a neuromuscular condition in which voluntary muscle contraction causes simultaneous involuntary contraction of other muscle groups e.g. pursing of the lips causes involuntary closure of the eye. It is a common sequelae of facial nerve paralysis with 55% or more of patients reporting synkinetic facial movement. 2 Additionally, patients may develop hyperkinesis due to continual firing of nerves that have aberrantly regenerated, thereby causing decreased movement due to antagonistic muscle hyperactivity, tightness, spasms, and pain. These together significant affect facial symmetry, aesthetics, and facial function.

While the definitive pathophysiology of synkinesis is still unknown, the most supported theory describes neuronal miswiring (aberrant regeneration theory). It suggests that following injury to the facial nerve and Wallerian degeneration, axons from the facial nucleus in the brainstem regrow and form inappropriate connections to peripheral muscle groups (e.g. a nerve meant to control the orbicularis oris of the mouth connects to the orbicularis oculi of the eye as well). This results in involuntary facial movements during normal expression and can affect all muscles of facial expression.

Furthermore, because of continual facial muscular tone or hypertonicity, this is not only a dynamic process, but a static one as well. Synkinesis and hypertonicity can cause facial asymmetry and a fixed immobile face ("frozen facies) due to opposing muscles constantly contracting and limiting movement. The result can be unaesthetic: the eyes may look smaller, the commissure (corner) of the mouth may look deviated up and out, the nasolabial fold may look deeper, the base of the nose may be deviated, the chin may be twisted or dimpled, and a band may be seen in the neck. This also presents functional limitations, such as difficulties in articulation, biting of the lip/cheek, nasal obstruction, incomplete oral competency with drooling, watering of the eye (epiphora) and in controlling facial expressions. Patients notice pain, tightness, poor facial movement, and difficulty expressing emotions, loss of their smile, and embarrassment. These limitations decrease confidence and ultimately the patient's quality of life.

Our study intends to look specifically at periocular synkinesis with orbicularis oculi muscle hypertonicity resulting in acquired blepharoptosis over time (i.e. drooping of the eyelid). Periocular synkinesis is partial closure of the eye due to inappropriate contraction of the orbicularis oculi muscle during other facial movement. Hypertonicity of the orbicularis oculi muscle results in the static narrowing of the palpebral fissure (acquired blepharoptosis) and may cause visual obstruction, asymmetry, and an aged appearance in the affected eye and can occur with both dynamic movement and static tone (hyperkinesis).

This facial movement disorder has no cure. Treatments are intended to improve facial symmetry, decreased tightness/pain, improve function and improve quality of life. These include facial therapy, chemodenervation injections with neurotoxins, and a variety of surgeries. Patients require multimodal therapy. None of these treatments adequately address the acquired blepharoptosis from chronic hyperkinesis and synkinesis.

Oxymetazoline was initially developed in 1961. It is a direct sympathomimetic, binding directly to alpha-1 and alpha-2 receptors. Currently, it is used as a nasal decongestant, in the treatment of epistaxis, and as a topical treatment for rosacea. Previously, an ophthalmic formulation was used to treat eye redness and irritation as it is FDA approved for the treatment of acquired blepharoptosis. However, this product line was discontinued when in July of 2020, oxymetazoline received Food and Drug Administration approval for treatment of cosmetic blepharoptosis.

In the treatment of blepharoptosis, oxymetazoline acts on the superior tarsal muscle, Müller's muscle, to elevate the eyelid. The superior tarsal muscle is a sympathetically innervated muscle that is partially responsible for elevating the eyelid. 5 Previous cosmetic studies have shown oxymetazoline can serve as an adjunct to botulinum toxin in patients with acquired blepharoptosis. However, no study has been performed evaluating oxymetazoline's efficacy as an adjunct to botulinum toxin in patients with acquired blepharoptosis secondary to hypertonicity and synkinesis.

02

Conditions studied

  • Blepharoptosis
  • Synkinesis
  • Hyperkinesis
  • Facial Paralysis

Keywords

  • acquired blepharoptosis
  • hyperkinesis
  • synkinesis
  • facial paralysis
  • aberrant regeneration syndrome
  • post-paralysis synkinesis
  • nonflaccid facial paralysis
03

In context

Blepharoptosis

75 studies on the registry are indexed under Blepharoptosis; 14 are open to participants now.

This study's enrollment of 36 is below the median of 50 across 56 interventional studies indexed under Blepharoptosis.

Browse Blepharoptosis studies →

Lead sponsor

Milton S. Hershey Medical Center is the lead sponsor of 492 studies on the registry; 60 are open to participants now.

Of its 58 completed or terminated interventional studies of FDA-regulated products, 46 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Over 18 years of age
  2. Primary diagnosis of nonflaccid facial paralysis (aberrant regeneration syndrome) and acquired blepharoptosis.

Exclusion criteria

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).
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Investigator)
Enrollment
36 participants (actual)

Study arms

  • Experimental
    Oxymetazoline 0.1% ophthalmic drops

    Patients will use once daily in affected eye. Drops are provided in single use vials.

    Drug: Oxymetazoline 0.1% (Pf) Oph Soln Ud

  • Placebo comparator
    Preservative free lubricating drops

    Patients will use once daily in affected eye. Drops are provided in single use vials.

    Other: Preservative free lubricating drops

Interventions

  • Oxymetazoline was initially developed in 1961. It is a direct sympathomimetic, binding directly to alpha-1 and alpha-2 receptors. Currently, it is used as a nasal decongestant, in the treatment of epistaxis, and as a topical treatment for rosacea. Previously, an ophthalmic formulation was used to treat eye redness and irritation as it is FDA approved for the treatment of acquired blepharoptosis. However, this product line was discontinued when in July of 2020, oxymetazoline received Food and Drug Administration approval for treatment of cosmetic blepharoptosis. In the treatment of blepharoptosis, oxymetazoline acts on the superior tarsal muscle, Müller's muscle, to elevate the eyelid. The superior tarsal muscle is a sympathetically innervated muscle that is partially responsible for elevating the eyelid. Previous cosmetic studies have shown oxymetazoline can serve as an adjunct to botulinum toxin in patients with acquired blepharoptosis.

    Also known as: Upneeq

  • OtherPreservative free lubricating drops

    Over the counter ophthalmic lubricating drop.

    Also known as: soothe

06

What researchers measure

Primary outcomes

  1. Difference from baseline to end of study in Sunnybrook Grading Score

    Clinician-graded outcome measure

    Time frame: 6 months

  2. Difference from baseline to end of study Synkinesis Assessment Questionnaire

    Patient reported outcome measure

    Time frame: 6 months

  3. Difference from baseline to end of study in Facial Disability Index

    Disease-specific quality of life measure

    Time frame: 6 months

Secondary outcomes

  1. Difference in MRD-1 from baseline to when medication is being used

    Objective assessment of eyelid position relative to the pupillary light reflex as measured by clinician

    Time frame: 6 months

  2. Difference in palpebral height from baseline to when medication is being used

    Width of ocular aperture from upper to lower eyelid

    Time frame: 6 months

07

Study locations

1 site
  • M.S. Hershey Medical Center
    Hershey, Pennsylvania 17033, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05945615
Responsible party
Jessyka Lighthall (Chief, Facial Plastic and Reconstructive Surgery, Associate Professor, Department of Otolaryngology-Head and Neck Surgery, Milton S. Hershey Medical Center) — Principal investigator
First posted
Jul 14, 2023
Start date
Jan 11, 2024
Primary completion
Jan 8, 2026
Completion
Jan 8, 2026
Last update
Mar 9, 2026

Study contacts

Jessyka Lighthall, MD
principal investigator · Penn State Health

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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Studies of the drug tested here: Oxymetazoline

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