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NCT02506348 Clinical Trial

Comparison of Diclofenac vs. Nepafenac Ophthalmic Drops: Patient Comfort

Pain Management Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02506348
Other study ID # 0011-15
Secondary ID
Status Recruiting
Phase N/A
First received July 2, 2015
Last updated July 22, 2015
Start date July 2015

Study information
Verified date July 2015
Source Wolfson Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

In this study we test Diclofenac and Nepafenac and compared patients experience and comfort following administration of these ophthalmic drops.

Description:

In this study we will compare the ocular tolerability between preservative-free Diclofenac and Nepafenac drops. Using a standard comparative scale we will measured discomfort, itching, burning and pain in intervals of 1 sec, 5 sec, 1 min and 5 min post-administration.

The results may aid both doctors and patients in decision regarding the post surgical anti-inflammatory treatment.

Recruitment information / eligibility
Status Recruiting
Enrollment 30
Est. completion date
Est. primary completion date January 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patient facing cataract surgery

Exclusion Criteria:

- under 18

- cognitive decline

Study Design

Intervention Model: Single Group Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

Intervention

Drug:
• Diclofenac

• Nepafenac

Locations
Country Name City State
Israel The E.Wolfson Medical Center Holon

Sponsors (1)
Lead Sponsor Collaborator
Wolfson Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary patient's comfort change in patient's comfort between both eyes at 1 min post administration 1 min post administration No
Secondary patient's comfort change in patient's comfort between both eyes at 10 min post administration 5 min post administration No
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