A Clinical Trial About Treatment of Mild to Moderate Persistent Alergic Rhinnitis With Test or Reference Mometasone (PUMA)
Primary Purpose
Mild to Moderate Persistent Allergic Rhinitis
Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Mometasone furoate
Mometasone furoate
Sponsored by
About this trial
This is an interventional treatment trial for Mild to Moderate Persistent Allergic Rhinitis
Eligibility Criteria
Inclusion Criteria:
- Sign and date the informed consent form or, in case of subjects younger than 18 years, the document must also be signed by a legal guardian;
- ≥ 12 years old;
- Suffer from mild to moderated persistent alergic rhinitis;
- Total NIS scale score ≥ 4 points at the screening visit and within at least 4 of the 7 days before the randomization visit;
- Indication for use nasal corticosteroid;
- Present with alergic rhinitis symptoms for at least 2 years;
- May undergo a washout period of at least 2 weeks
Exclusion Criteria:
- Patients with severe alergic rhinitis;
- Patients with severe co-morbidities (at the investigator's criteria);
- Patients with mild to severe persistent asthma;
- Clinical history of infection of the airways 30 days before the study entry;
- Patients with structural changes causing nasal obstruction, such as pronounced nasal septum deviation, nasal polyps or any other type of nasal malformation;
- For female subjects, be pregnant or breastfeeding or planning to become pregnant or unwilling to use safe birth control methods during the study;
- subjects in need of other drugs to treat alergic rhinitis, such as anti-immunoglobulin E, immunotherapy, anti-leukotrienes, oral corticosteroids, inhalant corticosteroids, or any administration route other than cutaneous;
- Active smokers (use of cigarette, pipe, cigar or any other form of tobacco in any amount within the past 3 months before the study entry);
- Participation in another clinical study within the past 12 months;
Sites / Locations
- IMA Brasil - Instituto de Pesquisa Clínica e Medicina Avançada
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Mometasone
Nasonex®
Arm Description
Outcomes
Primary Outcome Measures
Nasal Index Score (NIS) scale that evaluates nasal obstruction, coryza, and sneezing
Secondary Outcome Measures
Full Information
NCT ID
NCT01372865
First Posted
June 13, 2011
Last Updated
September 15, 2017
Sponsor
Eurofarma Laboratorios S.A.
1. Study Identification
Unique Protocol Identification Number
NCT01372865
Brief Title
A Clinical Trial About Treatment of Mild to Moderate Persistent Alergic Rhinnitis With Test or Reference Mometasone (PUMA)
Official Title
A Phase III, Non-inferiority, Open-label, Multicenter and Randomized Clinical Trial About the Treatment of Mild to Moderate Persistent Allergic Rhinitis With Eurofarma Mometasone or Reference Mometasone.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Completed
Study Start Date
June 2012 (Actual)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
March 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Eurofarma Laboratorios S.A.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary objective will be to compare the impact of the study formulations on alergic rhinitis carriers.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild to Moderate Persistent Allergic Rhinitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
364 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Mometasone
Arm Type
Experimental
Arm Title
Nasonex®
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Mometasone furoate
Intervention Type
Drug
Intervention Name(s)
Mometasone furoate
Primary Outcome Measure Information:
Title
Nasal Index Score (NIS) scale that evaluates nasal obstruction, coryza, and sneezing
Time Frame
04 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Sign and date the informed consent form or, in case of subjects younger than 18 years, the document must also be signed by a legal guardian;
≥ 12 years old;
Suffer from mild to moderated persistent alergic rhinitis;
Total NIS scale score ≥ 4 points at the screening visit and within at least 4 of the 7 days before the randomization visit;
Indication for use nasal corticosteroid;
Present with alergic rhinitis symptoms for at least 2 years;
May undergo a washout period of at least 2 weeks
Exclusion Criteria:
Patients with severe alergic rhinitis;
Patients with severe co-morbidities (at the investigator's criteria);
Patients with mild to severe persistent asthma;
Clinical history of infection of the airways 30 days before the study entry;
Patients with structural changes causing nasal obstruction, such as pronounced nasal septum deviation, nasal polyps or any other type of nasal malformation;
For female subjects, be pregnant or breastfeeding or planning to become pregnant or unwilling to use safe birth control methods during the study;
subjects in need of other drugs to treat alergic rhinitis, such as anti-immunoglobulin E, immunotherapy, anti-leukotrienes, oral corticosteroids, inhalant corticosteroids, or any administration route other than cutaneous;
Active smokers (use of cigarette, pipe, cigar or any other form of tobacco in any amount within the past 3 months before the study entry);
Participation in another clinical study within the past 12 months;
Facility Information:
Facility Name
IMA Brasil - Instituto de Pesquisa Clínica e Medicina Avançada
City
Sao Paulo
Country
Brazil
12. IPD Sharing Statement
Citations:
PubMed Identifier
26968623
Citation
Antila MA, Castro FM, Sano F, Machado A, Fernandes F, Rosario Filho NA, Stelmach R. Mometasone furoate in the treatment of mild, moderate, or severe persistent allergic rhinitis: a non-inferiority study (PUMA). Braz J Otorhinolaryngol. 2016 Sep-Oct;82(5):580-8. doi: 10.1016/j.bjorl.2015.11.009. Epub 2016 Feb 15.
Results Reference
derived
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A Clinical Trial About Treatment of Mild to Moderate Persistent Alergic Rhinnitis With Test or Reference Mometasone (PUMA)
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