CTRI/2024/05/067217
Not yet recruiting
Phase 4
A comparative study of the efficacy and safety of olopatadine 0.7% versusalcaftadine 0.25% in allergic conjunctivitis - NI
Pt B.D. Sharma UHS Rohtak0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Pt B.D. Sharma UHS Rohtak
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Positive medical history of mild to moderate ocular allergies.
- •\-Best corrected visual acuity of 6 by 12 or better in each eye.
- •\-Absence of contact lens use for a minimum of three days before and throughout the study period.
- •\-Willingness to provide informed consent
Exclusion Criteria
- •\-Diagnosis of persistent dry eye syndrome.
- •\-Use of any topical eye drops, including ocular lubricants, aside from the investigational drugs within the past seventy two hours, or utilization of any experimental medications or devices within the last thirty days.
- •\-Taking aspirin, or related products, systemic steroids or H1antihistamines within seven days prior to enrolment.
- •\-Presence of an active ocular infection.
- •\-Planned surgical procedures during the study period or recent ocular surgical intervention within three months.
- •\-Pregnancy and lactation
Outcomes
Primary Outcomes
Not specified
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