Comparison Between Dexchlorpheniramine and Dexchlorpheniramine/Pseudoephedrine/Guaifenesin in Respiratory Infections
Primary Purpose
Viral Infections of the Upper Respiratory Tract
Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Dexchlorpheniramine, pseudoephedrine, guaifenesin
Dexchlorpheniramine
Sponsored by

About this trial
This is an interventional treatment trial for Viral Infections of the Upper Respiratory Tract focused on measuring allergic rhinitis, viral infections of the upper respiratory tract, dexchlorpheniramine, pseudoephedrine, guaifenesin
Eligibility Criteria
Inclusion Criteria:
- Patients with allergic rhinitis with symptoms of viral infection of the upper respiratory tract (rhinorrhea, nasal obstruction and productive cough)
- Compliance of the subject to the treatment protocol
- Agreement with the terms of the informed consent
- Patients who did not use forbidden medications
Exclusion Criteria:
- History of allergy to any component of the formulations
- Use of any investigational drug within the last 30 days
- Patients with bacterial infections of the upper respiratory tract
- Patients with high blood pressure (> 140 x 90 mmHg)
- Patients who are receiving inhaled beta-agonists or other antihistamine, decongestant or expectorant
- Patients with known pulmonary disease (asthma, COPD, neoplasias)
- Pregnancy
- HIV + patients
- Other conditions considered by the investigator as reasonable for non-eligibility
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Dexchlorpheniramine pseudoephedrine guaifenesin
Dexchlorpheniramine
Arm Description
Outcomes
Primary Outcome Measures
Symptoms frequency and intensity evaluated with a 5 point visual analogic scale (VAS)
Secondary Outcome Measures
Subjective evaluation of efficacy and tolerability graded as excellent, good, fair ou poor.
Full Information
NCT ID
NCT01085721
First Posted
March 9, 2010
Last Updated
March 10, 2010
Sponsor
Mantecorp Industria Quimica e Farmaceutica Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT01085721
Brief Title
Comparison Between Dexchlorpheniramine and Dexchlorpheniramine/Pseudoephedrine/Guaifenesin in Respiratory Infections
Official Title
Comparison Between Dexchlorpheniramine and Dexchlorpheniramine/Pseudoephedrine/Guaifenesin in the Relief of Allergic Symptoms in Rhinitic Patients With Viral Upper Respiratory Tract Infections and Productive Cough
Study Type
Interventional
2. Study Status
Record Verification Date
March 2010
Overall Recruitment Status
Unknown status
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Mantecorp Industria Quimica e Farmaceutica Ltd.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Patients with allergic rhinitis frequently present exacerbation of the atopic symptoms during viral infections of the upper respiratory tract. Also, allergic rhinitis makes the mucosa more reactive to infectious agents and potentiates mucus production.
The combination of dexchlorpheniramine, pseudoephedrine and guaifenesin elicits antihistaminic, decongestant and expectorant effects. The study hypothesizes is that this product is superior to dexchlorpheniramine alone in the relief of allergic symptoms and in promoting mucus elimination in atopic patients with viral infections of the upper respiratory tract.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Viral Infections of the Upper Respiratory Tract
Keywords
allergic rhinitis, viral infections of the upper respiratory tract, dexchlorpheniramine, pseudoephedrine, guaifenesin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
170 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Dexchlorpheniramine pseudoephedrine guaifenesin
Arm Type
Experimental
Arm Title
Dexchlorpheniramine
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Dexchlorpheniramine, pseudoephedrine, guaifenesin
Intervention Description
5 mL (2 mg dexchlorpheniramine, 20 mg pseudoephedrine and 100 mg guaifenesin) qid for 5 days
Intervention Type
Drug
Intervention Name(s)
Dexchlorpheniramine
Intervention Description
5 mL (2 mg dexchlorpheniramine) qid for 5 days
Primary Outcome Measure Information:
Title
Symptoms frequency and intensity evaluated with a 5 point visual analogic scale (VAS)
Time Frame
5 days
Secondary Outcome Measure Information:
Title
Subjective evaluation of efficacy and tolerability graded as excellent, good, fair ou poor.
Time Frame
5 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with allergic rhinitis with symptoms of viral infection of the upper respiratory tract (rhinorrhea, nasal obstruction and productive cough)
Compliance of the subject to the treatment protocol
Agreement with the terms of the informed consent
Patients who did not use forbidden medications
Exclusion Criteria:
History of allergy to any component of the formulations
Use of any investigational drug within the last 30 days
Patients with bacterial infections of the upper respiratory tract
Patients with high blood pressure (> 140 x 90 mmHg)
Patients who are receiving inhaled beta-agonists or other antihistamine, decongestant or expectorant
Patients with known pulmonary disease (asthma, COPD, neoplasias)
Pregnancy
HIV + patients
Other conditions considered by the investigator as reasonable for non-eligibility
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Claudia Domingues
Phone
+551151885237
Email
cdomingues@mantecorp.com
12. IPD Sharing Statement
Learn more about this trial
Comparison Between Dexchlorpheniramine and Dexchlorpheniramine/Pseudoephedrine/Guaifenesin in Respiratory Infections
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