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NCT01128556

The Evaluation of the Effect of Bepreve, a Topical Ocular Antihistamine, on the Measurement of Wheal and Flare Response From Histamine Skin Prick Testing

Completed Phase 4 Last updated 7 July 2010
What this trial tests

Phase 4 trial testing Bepreve in Histamine Responsive Allergy Patients in 30 participants. Completed in 1 June 2010.

Timeline
1 April 2010
Primary endpoint
1 June 2010
1 June 2010

Quick facts

Lead sponsorNorth Texas Institute for Clinical Trials
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingnone
Enrollment30
Start date1 April 2010
Primary completion1 June 2010
Estimated completion1 June 2010
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

North Texas Institute for Clinical Trials

Who can join

Adults 18 to 65, any sex, with Histamine Responsive Allergy Patients. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

To evaluate the effect of BEPREVE compared to a REFRESH Tears Lubricant eye drop on the measurement of the wheal and flare from histamine skin prick testing. This is an open label, two-week, post-marketing study conducted on histamine responsive patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

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