Conjunctivitis, Allergic Clinical Trial
Official title:
A Double-blind, Placebo-controlled, Crossover, Single-center Study to Evaluate the Anti-allergic and Anti-inflammatory Effects of Multiple Doses of Desloratadine on Conjunctival Allergen Challenge-induced Ocular Signs and Symptoms
This study was a double-blind, placebo-controlled, cross-over, single-center study of desloratadine 5 mg or placebo in subjects 18 years of age or older with a history of seasonal allergic rhinoconjunctivitis. This study was performed to examine the effects of desloratadine compared with placebo, on the signs and symptoms of allergic conjunctivitis induced by direct conjunctival challenges with a previously identified sensitizing antigen, in the eyes of a subject known to be sensitive to the antigen.
n/a
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00501527 -
Immunotherapy With Depigmented and Polymerized Allergen Extract of Phleum Pratense
|
Phase 2 | |
Completed |
NCT00422149 -
Twin SUBLIVAC® Grasses Clinical Efficacy Study
|
Phase 3 | |
Completed |
NCT01470118 -
A Study to Evaluate the Duration of LASTACAFT® in Acute Allergic Conjunctivitis
|
Phase 4 | |
Completed |
NCT03709121 -
A Methodology Development Clinical Trial of Reproxalap in Subjects With Seasonal Allergic Conjunctivitis Using the Environmental Exposure Chamber
|
Phase 1/Phase 2 | |
Completed |
NCT02555761 -
Safety and Efficacy of Lastacaft® for the Prevention of Itching Associated With Allergic Conjunctivitis in Korea
|
||
Completed |
NCT01732757 -
A Study to Evaluate the Efficacy of Lastacaft® Compared to Patadayâ„¢ and Placebo in Patients With Acute Allergic Conjunctivitis
|
Phase 4 | |
Recruiting |
NCT04299399 -
Corneal Biomechanical Changes of Allergic Conjunctivitis
|
||
Completed |
NCT00917488 -
Glycyphagus Domesticus Allergen Extract. Determination of the in Vivo Biological Activity in Histamine Equivalent Units (HEP).
|
Phase 2 | |
Completed |
NCT03375775 -
Evaluation of Subcutaneous Immunotherapy Towards Pollen in Children
|
N/A | |
Completed |
NCT02082262 -
AGN-229666 Ophthalmic Solution for the Treatment of Seasonal or Perennial Allergic Conjunctivitis
|
Phase 3 | |
Withdrawn |
NCT01541904 -
Efficacy and Safety of PRO-118 Ophthalmic Solution in Allergic Conjunctivitis
|
Phase 2 | |
Completed |
NCT02161146 -
AGN-229666 Ophthalmic Solution in Japanese Patients With Allergic Conjunctivitis
|
Phase 3 | |
Completed |
NCT00718744 -
Standardization of Chortoglyphus Arcuatus Allergenic Extract. Determination of Biological Activity in HEP Units
|
Phase 2 | |
Recruiting |
NCT03186755 -
Clinical Evaluation of Hylo-Dual Versus Patanol in Children With Seasonal Allergic Conjunctivitis
|
Phase 4 | |
Completed |
NCT01987765 -
Safety and Efficacy of Relestat Ophthalmic Solution 0.05% for Allergic Conjunctivitis in Korea
|
N/A | |
Completed |
NCT06063044 -
Food-specific IgG4-guided Elimination Diets Improve Allergy Symptoms in Children
|
||
Completed |
NCT01289431 -
Mapracorat Ophthalmic Formulation in Subjects With Allergic Conjunctivitis
|
Phase 2 | |
Completed |
NCT00655109 -
A Comparison of Olopatadine and Fluticasone in Patients With Allergic Conjunctivitis
|
Phase 4 | |
Completed |
NCT00424398 -
Evaluation of the Onset and Duration of Action of Bepotastine Besilate Ophthalmic Solution in Acute Allergic Conjunctivitis
|
Phase 2/Phase 3 | |
Completed |
NCT03012165 -
A Study of ADX-102 in Subjects With Allergic Conjunctivitis
|
Phase 2 |