Clinical Trial: Nasya in Allergic Rhinitis

Study Status: Completed
Recruit Status: Completed
Study Type: Interventional

Official Title: Double-blind, Randomized, Placebo-controlled, Crossover Clinical Investigation to Evaluate Safety and Efficacy of Nasya in Reducing Symptoms of Allergic Rhinitis When Appl

Brief Summary: The purpose of this study is to evaluate safety and efficacy of Nasya in reducing symptoms of persistent allergic rhinitis when applied before allergen challenge.

Detailed Summary:
Sponsor: InQpharm Group

Current Primary Outcome: Difference in Total Nasal Symptom Score [ Time Frame: 75 minutes ]

Original Primary Outcome: Same as current

Current Secondary Outcome:

  • Difference in Total Nasal Symptom Score [ Time Frame: Up to 240 minutes ]
  • Difference in Total Ocular Symptom Score [ Time Frame: Up to 240 minutes ]


Original Secondary Outcome: Same as current

Information By: InQpharm Group

Dates:
Date Received: December 27, 2011
Date Started: January 2012
Date Completion:
Last Updated: October 25, 2012
Last Verified: October 2012