Eye drops may ease pain in second cataract surgery
NCT ID NCT07291089
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether anti-inflammatory eye drops (pranoprofen or prednisolone acetate) can reduce pain during second-eye cataract surgery compared to standard lubricating drops. 126 adults aged 50 and older who had already had one cataract surgery received the drops before their second surgery. The main goal was to see how many people reported significant pain (score 3 or higher on a 0-10 scale) within an hour after surgery.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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126 people
The number who actually took part.
- Started
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Feb 2024
- Finished
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Dec 2025
- 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.
- Ages
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50 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: * Aged ≥ 50 years. * Definite diagnosis of age-related cataract. * The first-eye cataract surgery under local anesthesia has been completed at this hospital, and the second-eye cataract surgery under local anesthesia is planned with the same surgeon within 1 year of the first-eye surgery. * Able to cooperate with preoperative iris optical coherence tomography angiography (OCTA) examination of the operative eye. * On the day of the second-eye surgery, preoperative iris vascular area density (VAD) ≥ 0.2167 in the operative eye. Exclusion Criteria: * History of ocular trauma, ocular surgery (excluding the first-eye cataract surgery already performed), uveitis, chorioretinal disease, glaucoma; * Presence of significant corneal disease, marked iris abnormalities, or any active ocular surface disease, including recent conjunctivitis, keratitis, or severe dry eye. * Severe complications during or after the first-eye surgery (e.g., posterior capsule rupture, zonular dialysis, dislocation of the lens nucleus into the vitreous cavity, postoperative endophthalmitis, or glaucoma). * History of chronic pain syndromes or neuropathic pain. * Long-term use of opioids, other systemic analgesics, or sedative-hypnotic drugs. * Known autoimmune disease or ongoing immunosuppressive therapy. * Severe psychiatric disorders or cognitive impairment interfering with pain assessment. * Use of topical corticosteroid eye drops in the second eye within 1 month prior to the planned surgery. * Long-term use of α-adrenergic blockers or other medications associated with intraoperative floppy iris syndrome (IFIS). * Participation in any other clinical trial involving ophthalmic or systemic drugs within the past 6 months. * Known allergy or contraindication to topical nonsteroidal anti-inflammatory drugs (NSAIDs) (e.g., pranoprofen) or topical corticosteroids (e.g., prednisolone acetate) used in this study.
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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
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Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai, Shanghai Municipality, 200080, China
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Other studies related to the condition(s) this trial covers.
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