Allergic Rhinitis
Conditions
Keywords
Allergic Rhinitis
Brief summary
The purpose of this study is to evaluate the efficacy and safety of Magnólia nasal gel in the treatment of moderate-severe persistent or moderate-severe intermittent allergic rhinitis.
Interventions
DRUGMAGNÓLIA NASAL GEL
Magnólia nasal gel spray
DRUGMOMETASONE FUROATE
Mometasone furoate nasal spray
Sponsors
EMS
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Ability to confirm voluntary participation and agree to all trial purposes by signing and dating the informed consent forms; * Participants of both sexes, with age greater than or equal to 12 years; * Clinical diagnosis of moderate-severe persistent or moderate-severe intermittent allergic rhinitis, according to the ARIA classification; * Present the general status of rhinitis as moderate or severe; * Total nasal symptom score greater than or equal to 6 points, with congestion and one or more of the other symptoms present (itching, runny nose, and sneezing) with a score greater than or equal to 2 at the screening visit; * Present skin sensitization test to at least one aeroallergen;
Exclusion criteria
* Any clinical and laboratory findings that, in the judgment of the investigator, may interfere with the safety of research participants; * History of alcohol abuse or illicit drug use; * Participation in a clinical trial in the year before this study; * Pregnancy or risk of pregnancy and lactating patients; * Known hypersensitivity to the formula components used during the clinical trial; * Participants who present other clinical forms of rhinitis, such as, but not restricted to medicated rhinitis, vasomotor and atrophic; * Participants dependent on decongestants (nasal or oral) or receiving allergen-specific immunotherapy; * Participants with suggestive signs of upper airways bacterial infection; * Participants with grade II or III septum deviation and/or presence of nasal polyps or other conditions that lead to nasal obstruction; * Concomitant chronic or intermittent use of decongestants, antihistamines, or corticosteroids by inhalation, oral, intramuscular, or intravenous; * Concomitant use of potent topical corticosteroids.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from baseline in the reflective total nasal symptom score (rESN) averaged over the entire treatment period. | 4 weeks | The participant will answer the nasal symptom score (together with their parents or guardians, for participants with less than 18 years old) every 12 hours, in the participant's diary. The rESN will be the average of the two measurements of the day. |
Secondary
| Measure | Time frame |
|---|---|
| Incidence and severity of adverse events recorded during the study. | 6 to 10 weeks |
Outcome results
None listed