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Topical nonsteroidal anti-inflammatory drug effect on patients with pseudoexfoliation syndrome during cataract surgery

The role of topical NSAIDs on inflammation and anterior segment complications after cataract surgery in patients with pseudoexfoliation syndrome

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160919029871N3
Enrollment
96
Registered
2018-03-02
Start date
2018-01-21
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Anterior segment inflammation and complications after cataract surgery in patients with pseudoexfoliation syndrome. Age-related cataract

Interventions

Intervention 1: Interventional Group: In addition to routine care including chloramphenicol eye drops every 6 hours and betamethasone eye drops every 4 hours until one month after surgery, ketorolac (

Sponsors

Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 95 Years

Inclusion criteria

Inclusion criteria: Having Significant cataract (grade 3 and higher) and clinical signs of PEX. The patient should not be used systemic or inhaled NSAIDs within 1 week before surgery and the patients should not use the inhaled or systemic corticosteroids within 15 days after surgery

Exclusion criteria

Exclusion criteria: Having known hypersensitivity to any components of the NSAIDs uncontrolled chronic ocular or systemic inflammatory disease; a history of eye trauma and any retinal and macular disease, any intraocular complication during surgery (vitreous loss) The patient who must be treated with systemic anti-inflammatory medications for extensive inflammation following cataract surgery

Design outcomes

Primary

MeasureTime frame
Percentage of subjects with anterior chamber inflammation based on cell count (CELL) and percentage of subjects with anterior chamber inflammation based on protein content based on the rating of the San-working Group (0 to 4 degrees). Timepoint: 1, 3, 7 and 30 days after surgery. Method of measurement: Clinical examination.

Secondary

MeasureTime frame
The degree of opacity of the anterior capsule (ACO) (grade 0-4) and degree of opacity of the posterior capsule (PCO) (grade 0-4). Timepoint: 1,3,6 months postoperatively. Method of measurement: photo slit examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mitra Akbari

Guilan University of Medical Sciences

mitra.akbari20@gmail.com+98 13 3323 6886

Outcome results

None listed

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