Could years of eye injections weigh down the upper eyelid?
NCT ID NCT07821450
First seen Sep 15, 2026 · Last updated Sep 16, 2026 · Updated 1 time
Summary
Doctors use anti-VEGF injections to treat retinal diseases such as age-related macular degeneration and diabetic macular edema, and patients often need these shots for years. During each injection, a small tool holds the eyelids open, stretching the upper lid. Researchers want to know whether this repeated stretching changes eyelid position over time. The study follows 60 adults who are starting injections in one eye only, using the untreated eye as a comparison, and measures eyelid height and muscle function at set visits over 12 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If repeated injections do affect eyelid position, doctors could adjust how they hold the eyelid open or counsel patients about this possible side effect.
- What could go wrong
- This is a small observational study at one center, so any link it finds may not hold up in larger or more varied groups. It cannot prove that injections cause eyelid drooping.
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.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2028
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
Adults aged 18 years or older with a retinal disease (neovascular age-related macular degeneration, diabetic macular edema or retinal vein occlusion) scheduled to begin intravitreal anti-VEGF therapy in one eye only, with no history of intravitreal injection in either eye, recruited consecutively at a single tertiary ophthalmology clinic in Istanbul, Turkey.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Age 18 years or older * Planned initiation of intravitreal anti-VEGF injection in one eye only for a retinal disease * No prior intravitreal injection in either eye * Able to attend the scheduled follow-up visits and to cooperate for the duration of the study * Reliable MRD-1, MRD-2 and levator function measurement possible in both eyes (clear corneal light reflex, clearly visible eyelid margin, able to maintain primary gaze) * Signed informed consent Exclusion Criteria: * Pre-existing blepharoptosis or significant eyelid malposition at the baseline examination * Previous ptosis surgery, blepharoplasty or other eyelid surgery that may affect upper eyelid anatomy * History of myasthenia gravis, oculomotor nerve palsy, Horner syndrome, facial nerve palsy or a similar neurologic or neuromuscular disorder * History of orbital trauma, orbital surgery or orbital disease * Advanced dermatochalasis, eyelid retraction, entropion, ectropion or marked facial asymmetry precluding reliable eyelid measurement * Need for intravitreal injection in both eyes during the study period * Ocular or periocular surgery during follow-up that may affect upper eyelid position * Inability to comply with follow-up visits or incomplete measurements * Withdrawal of consent * Inability to obtain reliable eyelid measurements due to severe blepharospasm, advanced corneal opacity, marked eyelid edema, or inability to maintain head or neck position or to cooperate
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Health Sciences, Fatih Sultan Mehmet Training and Research Hospital
Istanbul, Turkey (Türkiye)
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