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Non-steroidal anti-inflammatory (NSAID) medication in cataract surgery

Non-steroidal anti-inflammatory medication in cataract surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2015-005313-79-FI
Enrollment
100
Registered
2016-11-01
Start date
2017-01-05
Completion date
Unknown
Last updated
2024-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract senilis

Interventions

Trade Name: Dicloabak Product Name: Dicloabak Pharmaceutical Form: Eye drops, solution CAS Number: 15307-81-0 Other descriptive name: DICLOFENAC POTASSIUM Trade Name: Nevanac Product Name: Nevanac 1m

Sponsors

Raimo Tuuminen
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Age 60-90 years Fullfills national criteria for cataract surgery Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 20 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 80

Exclusion criteria

Exclusion criteria: active wet AMD /planned anti-VEGF therapy prior retinal vein/artery occlusiion, retinal detachment, optic neuritis, vitreous hemorrhage, intraocular surgery. Myopia magna. Pregnancy. Alcohol misuse.

Design outcomes

Primary

MeasureTime frame
Main Objective: To study efficacy different nonsteroidal anti-inflammatory eye drops in management of post-operative inflammation and prevention of pseudophakic cystic macular edema after uncompplicated cataract surgery;Secondary Objective: To study efficacy different nonsteroidal anti-inflammatory eye drops in prevention of posterior capsule opacification after uncompplicated cataract surgery;Primary end point(s): Best corrected visual acuity, intraocular pressure, central retinal thickness, aqueous flare;Timepoint(s) of evaluation of this end point: 1 month

Secondary

MeasureTime frame
Secondary end point(s): Best corrected visual acuity, intraocular pressure, central retinal thickness, aqueous flare;Timepoint(s) of evaluation of this end point: 3 month

Countries

Finland

Contacts

Public ContactClinical Trials Information

Raimo Tuuminen

raimo.tuuminen@helsinki.fi358504113870

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026