Safety and Efficacy of Lastacaft® for the Prevention of Itching Associated With Allergic Conjunctivitis in Korea
- 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
-Patients with itching associated with allergic conjunctivitis.
-Patients with hypersensitivity to Lastacaft® or its components.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description 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
Name Time Method Number of Participants with Adverse Events 2 Weeks
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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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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