Study to Evaluate the Efficacy and Safety of Fixed Dose Combination of Diphenhydramine + Pseudoephedrine + Dropropizine in the Control of Cough and the Relief of Nasal Symptoms, Suffering From Non-productive Cough and Acute Rhinitis

NCT ID: NCT01199497

Last Updated: 2017-07-13

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE3
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-08-31
• Study Completion Date: 2013-01-31

Brief Summary

Multicenter clinical trial, phase III, controlled by active medicine, double-blind, randomized, enroll 208 subjects, above 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.

Conditions

Nasal Congestion; Cough

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Group 1

Fixed dose combination of diphenhydramine + dropropizine + pseudoephedrine (Notuss® syrup).

Group Type: EXPERIMENTAL

Group 1

Intervention Type: DRUG

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

Group 2

Placebo

Group Type: PLACEBO_COMPARATOR

Group 2

Intervention Type: DRUG

placebo

Interventions

Group 1

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

Intervention Type: DRUG

Group 2

placebo

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients over 12 years old, of both sexes;

2. Clinical condition compatible with acute rhinitis accompanied by nasal congestion;

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 congestion severity score (As per item 4.1.3);

6. If necessary, ICF signed by a parent/representant, or in case the patient over 18 years old, his own signature;

7. Patient and/or 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 (axilar 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. Female patients with positive b-HCG;

5. Patients under treatment for chronic allergy;

6. Presence of purulent or mucupurulent secretion, nasal vault or mal formations (cleft lip or cleft nasolabial corrected or not) in nasal vestibule;

7. Current use of systemic antibiotics for any reason;

8. Use of prohibited medicine within the prescribed period before V0 as shown in item 9.3 of this protocol;

9. Participation in last one year of clinical protocols;

10. Any psychiatric diseases, including major depression;

11. Presence of mental retardation from any cause;

12. Diagnosis of renal or hepatic failure;

13. History of hypersensitivity to any component of the study drugs;

14. Relatives of sponsor´s or study site´s employee;

15. Current evidence of clinically significant diseases: hematopoietic, gastrointestinal, cardiovascular, hepatic, renal, neurological, endocrine, psychiatric, autoimmune, pulmonary, or another disease that block the patient participation;

16. Patient or parent/representant with a history of lack of compliance to treatment or previous treatment protocols;

17. 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.

• Minimum Eligible Age: 12 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ache Laboratorios Farmaceuticos S.A.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

ACH-NTS-03(08/10)

Identifier Type: -

Identifier Source: org_study_id