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Safety and Efficacy of Lastacaft® for the Prevention of Itching Associated With Allergic Conjunctivitis in Korea

Completed
Conditions
Conjunctivitis, Allergic
Interventions
Registration Number
NCT02555761
Lead Sponsor
Allergan
Brief Summary

This post-marketing surveillance study will assess the safety and efficacy of Lastacaft® Opthalmic Solution 0.25% (Alcaftadine) for the prevention of itching associated with Allergic Conjunctivitis as prescribed as standard of care in clinical practice in Korea.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3423
Inclusion Criteria

-Patients with itching associated with allergic conjunctivitis.

Exclusion Criteria

-Patients with hypersensitivity to Lastacaft® or its components.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Lastacaft®Alcaftadine Ophthalmic Solution 0.25%One drop of Lastacaft® Ophthalmic Solution 0.25% (Alcaftadine) in each eye daily as prescribed as standard of care in clinical practice.
Primary Outcome Measures
NameTimeMethod
Number of Participants with Adverse Events2 Weeks
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (76)

Seo-myeon St.Mary's Hospital

🇰🇷

Busan, Korea, Republic of

SeoMyeon St. Eye Clinic

🇰🇷

Busan, Korea, Republic of

Inje University Busan Paik Hospital

🇰🇷

Busan, Korea, Republic of

Soojung Eye Hospital

🇰🇷

Busan, Korea, Republic of

Inje University Haeundae Paik Hospital

🇰🇷

Busan, Korea, Republic of

Saint Mary Bright Eye Clinic

🇰🇷

Busan, Korea, Republic of

Daeyeon St.mary's Eye Center

🇰🇷

Busan, Korea, Republic of

Dong-A University Hospital

🇰🇷

Busan, Korea, Republic of

Pusan National University Hospital

🇰🇷

Busan, Korea, Republic of

Pusan National University Yangsan Hospital

🇰🇷

Busan, Korea, Republic of

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Seo-myeon St.Mary's Hospital
🇰🇷Busan, Korea, Republic of

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