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Alcaftadine vs Bepotastine which eyedrop wins the allergy battle

A Comparative Analysis on The Safety and Efficacy Of Alcaftadine 0.25 percentage and Bepotastine Besilate 1.5 percentage Eye Drop In The Of Allergic Conjunctivitis In Tertiary Hospital Kanpur - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099913
Enrollment
150
Registered
2025-12-29
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H102- Other acute conjunctivitis

Interventions

Intervention1: Antihistaminic - Topical Alcaftadine 0.25%: Topical Alcaftadine 0.25% eyedrop once a day for 14 days Control Intervention1: Antihistaminic- Topical Bepotastine besilate 1.5%: Topical Be

Sponsors

Rama medical College Hospital and Research Centre ,Kanpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Mild to moderate allergic conjunctivitis 2.Patient with both the sexes in ages18-60 years of age 3.Having one or more clinical feature of allergic conjunctivitis such as Itching, Tearing , Redness , Swelling according to TOSS (grade 1+ and grade 2+) and hyperemia score grade 0.5 and 2. 4. willing to give written informed consent

Exclusion criteria

Exclusion criteria: 1.Patients with severe allergic conjunctivitis, need for topical steroids or topical immunosuppressive 2.TOSS grade 3 + and hyperemia score grades 3 i.e severe allergic conjunctivitis will be excluded 3.Contact lens wearers 4.Patients with an intra-ocular pressure of more than 21 mm Hg in either eye or any type of glaucoma 5.History of hypersensitivity to the study medications or their components (including benzalkonium chloride) 6.History of an ocular herpetic infection 7.An active ocular infection 8.Any significant systemic illness (eg. Hypertension, T2DM, CAD, CKD) 9.Taking systemic steroids or oral antihistamines currently or within 7 days prior to enrolment 10.Pregnant women, planning pregnancy, / lactating 11.use of any other topical ocular medications were excluded from the study.

Design outcomes

Primary

MeasureTime frame
TOSS SCORE, Hyperemia score Physical examination Ophthalmologic examinationTimepoint: day0 , day7 and day 14

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactDr Mohammd Waseem Khan

Rama Medical College Hospital and Research Centre, Kanpur

drkritijalota@gmail.com7393008710

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026