check_circleStudy Completed
Rhinitis, Allergic
Bayer Identifier:
19880
ClinicalTrials.gov Identifier:
EudraCT Number:
Not Available
EU CT Number:
Not Available
A study to evaluate changes in nasal airflow of Loratadine/Pseudoephedrine tablet and Fluticasone Propionate nasal spray in subjects following allergen exposure
Trial purpose
The purpose of the study is to evaluate changes in nasal airflow caused by loratadine 5 mg/pseudoephedrine sulfate 120 mg (Claritin D) tablet and fluticasone propionate 50 mcg per spray nasal spray (Flonase) in subjects suffering from nasal congestion and other allergy symptoms.
Key Participants Requirements
Sex
AllAge
18 - 65 YearsTrial summary
Enrollment Goal
82Trial Dates
February 2018 - May 2018Phase
Phase 4Could I Receive a placebo
YesProducts
Claritin-D® (Loratadine + Pseudoephedrine sulfate, BAY818725)Accepts Healthy Volunteer
NoWhere to participate
Status | Institution | Location |
---|---|---|
Completed | Kingston General Hospital | Kingston, K7L 2V7, Canada |
Primary Outcome
- Average percent change in PNIF (Peak Nasal Inspiratory Flow) from 0 to 4 hours after dosingdate_rangeTime Frame:Up to 4 hours
Trial design
Trial Type
InterventionalIntervention Type
DrugTrial Purpose
TreatmentAllocation
RandomizedBlinding
N/AAssignment
Crossover AssignmentTrial Arms
4