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NCT00489398 Clinical Trial

Comparison of CL Wear Between Two Allergy Drops

Allergic Conjunctivitis Clinical Trial

Official title:
Comparison of CL Wear Between Epinastine Hydrochloride and Olopatadine Hydrochloride

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00489398
Other study ID # 5316
Secondary ID
Status Withdrawn
Phase Phase 4
First received June 19, 2007
Last updated October 5, 2010
Start date July 2007
Est. completion date December 2008

Study information
Verified date October 2010
Source Hom, Milton M., OD, FAAO
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Comparison of two allergy drops for enhancing comfort and performance of contact lens wear

Description:

Contact lens patients will instill allergy drops and subjective and objective tests will be performed

Recruitment information / eligibility
Status Withdrawn
Enrollment 25
Est. completion date December 2008
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Males or females > 18 years old

- Mild to moderate dry eye symptoms

- Likely to complete all study visits and able to provide informed consent

Exclusion Criteria:

- Current use of topical cyclosporine

- Known contraindications to any study medication or ingredients

- Active ocular diseases or uncontrolled systemic disease (blepharitis patients that are actively being treated or disease that is uncontrollable)

- Ocular surgery within the past 3 months

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• epinastine HCL and olopatadine HCL

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Hom, Milton M., OD, FAAO Merck Sharp & Dohme Corp.

Outcome
Type Measure Description Time frame Safety issue
Primary Contact lens objective and subjective clinical performance testing up to 3 months
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