drugset / Trial / NCT02175485
Evaluation of Efficacy of Dellegra in Exposure Unit
NaSingle-groupOpen-labelTreatment
Summary
Primary Objective: To collect and analyze clinical data of Allergic Rhinitis patients' Total Nasal Symptom Score (TNSS) change after Dellegra internal use under high density pure Japanese cedar pollen exposure. Secondary Objective: To collect and analyze clinical data of Allergic Rhinitis patients' change in Total Symptom Score (TSS) and amount of nasal discharge, safety, and overall patients' impression about efficacy of Dellegra after Dellegra internal use under high density pure Japanese cedar pollen exposure.
Timeline
- Start
- 2014-06
- Primary completion
- 2014-06
- Completion
- 2014-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Fexofenadine | Unknown | 60 mg | Oral |
| Subject | Pseudoephedrine | Small molecule | 120 mg | Oral |