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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
Eurofarma Laboratorios S.A.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mild to Moderate Persistent Allergic Rhinitis

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
June 13, 2011
Last Updated
September 15, 2017
Sponsor
Eurofarma Laboratorios S.A.
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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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