Inflammation | Evaluation of Efficacy and Safety in Control Cough and the Relief of Nasal Symptoms in Children 2-12 Years Old,Suffering From Cough and Acute Rhinitis

Inflammation research study

What is the primary objective of this study?

Multicenter clinical trial, phase III, controlled by active medicine, open, randomized, enroll 962 children, 2 to 12 years old, that suffer acute inflammation upper airway characterized by non-productive cough, daytime/nighttime, with duration for at least 3 and no more than 5 consecutive days (without systemic/topic use of medication during this period) followed by nasal congestion, with or without associate other nasal symptoms (sneezing, runny nose, nasal itching and/or mouth breathing). The subjects will be allocated in 2 parallel groups, and will receive the medicines of study, according of the randomization.

Who is eligible to participate?

Inclusion Criteria: 1. Patients between 2 and 12 years old, of both sexes; 2. Clinical condition compatible with acute rhinitis accompanied by nasal obstruction; 3. Non-productive cough, daytime and/or nighttime with at least 3 and up 5 consecutive days in duration; 4. Score greater than or equal to 3 points on the cough severity score (As per item 4.1.2); 5. Score greater than or equal to 2 points on the nasal obstruction severity score (As per item 4.1.3); 6. ICF signed by a parent/caregiver/representant; 7. Parent/Caregiver/Representant capacity, according to investigator evaluation, for compliance at the treatment and protocol requirements, fulfilling the regular visits; Exclusion Criteria: 1. Non-productive cough with purulent smear, fever (axillar temperature superior than 37,8°C/100°F), purulent runny nose and other signs and symptoms of bacteria infection of upper and lower airways at 7 days before the screening/randomization visit; 2. Septal deviation level III (in any region and any nasal cavity) and/or nasal polyps or other determinants conditions of nasal congestion; 3. Previous diagnosis of asthma; 4. Patients under treatment for chronic allergy; 5. Presence of purulent or mucopurulent secretion, nasal vault or mal formations (cleft lip or cleft nasolabial corrected or not) in nasal vestibule; 6. Current use of systemic antibiotics for any reason; 7. Use of prohibited medicine within the prescribed period before V0 as shown in item 9.3 of this protocol; 8. Participation in last one year of clinical protocols; 9. Any psychiatric diseases, including major depression; 10. Presence of mental retardation from any cause; 11. Diagnosis of renal or hepatic failure; 12. History of hypersensitivity to any component of the study drugs; 13. Relatives of sponsor´s or study site´s employee; 14. Current evidence of clinically significant diseases: hematopoietic, gastrointestinal, cardiovascular, hepatic, renal, neurological, endocrine, psychiatric, autoimmune, pulmonary, or another disease that block the patient participation; 15. Patient or parent/caregiver/representant with a history of lack of compliance to treatment or previous treatment protocols; 16. Any finding of clinical observation (anamnesis and physical exam) laboratory abnormality (eg, blood glucose, blood count), disease (for example, liver, cardiovascular system, lung) or therapy that, in opinion of the investigator, may endanger the patient or interfere with the endpoints of study.

Which medical condition, disease, disorder, syndrome, illness, or injury is researched?




Study Interventions

Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.

Drug:diphenhydramine + dropropizine + pseudoephedrineGroup 1: fixed dose combination of diphenhydramine + dropropizine + pseudoephedrine (Notuss® syrup). Posology: The medicine treat will be as follows: - Notuss® syrup Age: 2-5 years / Dosage: 5,0 mL Age: 6-12 years / Dosage: 10,0 ml

Drug:Dropropizine and fixed dose combination of pseudoephedrine hydrochloride + brompheniramine maleate (Dimetapp® elixir).Dropropizine: Age: 2 - 3 years / Dosage: 5,0 ml Age: 4 - 12 years / Dosage: 10,0 ml Pseudoephedrine hydrochloride + brompheniramine maleate: Age: 2 - 3 years / Dosage: 2,5 ml Age: 4 - 6 years / Dosage: 5,0 ml Age: 7 - 9 years / Dosage: 7,5 ml Age: 10 - 12 years / Dosage: 10,0 ml

Study Arms

Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.

Notuss® syrupGroup 1: fixed dose combination of diphenhydramine + dropropizine + pseudoephedrine (Notuss® syrup).

Dropropizine + Pseudoephedrine and brompheniramineGroup 2: combined use of dropropizine and fixed dose combination of pseudoephedrine hydrochloride + brompheniramine maleate.

Study Status


Start Date: October 2011

Completed Date:

Phase: Phase 3

Type: Interventional


Primary Outcome: Improvement of nasal congestion and cough

Secondary Outcome: Improvement of nasal congestion and cough

Study sponsors, principal investigator, and references

Principal Investigator:

Lead Sponsor: Ache Laboratorios Farmaceuticos S.A.


More information:

Discuss Cough