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Proof of concept trial of bromfenac ophthalmic solution for inhibitory effect against inflammatory cytokines.

Proof of concept trial of bromfenac ophthalmic solution for inhibitory effect against inflammatory cytokines. - Proof of concept trial of bromfenac ophthalmic solution for inhibitory effect against inflammatory cytokines.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000017934
Enrollment
30
Registered
2015-08-24
Start date
2015-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients with pseudophakic eye

Interventions

0.1% bromfenac sodium ophthalmic solution
One drop once, twice a day, instilled for 8 days 0.02% fluorometholone ophthalmic suspension
One drop once, twice a day, instilled for 8 days

Sponsors

Department of Ophthalmology, Faculty of Medical Science, University of Fukui
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients with the document agreement 2)Pseudophakic eye 3)Patients with the periods of three months or more after the end of the instillation of steroid and NSAIDs ophthalmic solution for post cataract operation

Exclusion criteria

Exclusion criteria: 1)Patients with a history of hypersensitivity against bromfenac and fluorometholone 2)Patients with ocular infections and inflammation (including allergic conjunctivitis and vernal keratoconjunctivitis) 3)Patients who received the ophthalmic surgery (including laser) within three months. 4)Patients with systemic diseases that may affect the efficacy or safety of the test drugs 5)Patients who was judged to be inappropriate as a subject by doctor in charge

Design outcomes

Primary

MeasureTime frame
Comparison of the cytokine concentration difference (before and 8 days after drug administration) between test drug groups

Secondary

MeasureTime frame
Comparison of the cytokine concentration between before and 8 days after drug administration in the same group

Countries

Japan

Contacts

Public ContactTakehiro Matsumura

University of Fukui, Faculty of medicine Ophthalmology

tmatsu@u-fukui.ac.jp0776-61-8403

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026