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Rinitis y Sinusitis según la Gravedad Del Asma (IRIS-ASMA)

This study has been completed.
Sponsor:
Collaborator:
Sociedad Española de Neumología y Cirugía Torácica
Information provided by (Responsible Party):
José Antonio Castillo Vizuete, Sociedad Española de Neumología y Cirugía Torácica
ClinicalTrials.gov Identifier:
NCT01513837
First received: January 17, 2012
Last updated: September 7, 2012
Last verified: September 2012
History of Changes
  Purpose

Based on the evidence for the "common pathway" in asthma presentation, our working hypothesis is that asthma severity and lack of control are related to the prevalence and severity of nasal and sinusal inflammatory pathology, and especially to chronic rhinosinusitis with nasal polyps.


Condition
Asthma

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: PREVALENCIA, GRAVEDAD E IMPACTO DE LA RINITIS Y DE LA SINUSITIS SEGÚN EL NIVEL DE GRAVEDAD Y CONTROL DEL ASMA (PROYECTO IRIS-ASMA)

Resource links provided by NLM:

MedlinePlus related topics: Asthma Sinusitis
U.S. FDA Resources

Further study details as provided by Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau:

Estimated Enrollment: 450
Study Start Date: March 2011
Study Completion Date: September 2012
Primary Completion Date: February 2012 (Final data collection date for primary outcome measure)
Detailed Description:

Primary objective: To assess the prevalence and severity of rhinitis and rhinosinusitis, with or without nasal polyposis, in asthmatic patients depending on severity of their disease.

Secondary objectives:

To assess the impact of nasal and sinusal pathology on asthma control.

To correlate asthma severity to rhinitis and rhinosinusitis.

To compare the potential association between chronic rhinosinusitis, with and without nasal polyposis, and asthma severity, and to detect radiographic differences, markers of atopy, and pulmonary function.

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Hospitals in Spain and Latin America

Criteria

Inclusion Criteria:

  • Patients of both sexes aged 18‐70 years attending outpatient clinics diagnosed with asthma at least one year before. GINA/GEMA criteria will be used to diagnose asthma and to rate its severity.

Exclusion Criteria:

  • Illiterate patients;
  • very severe, disabling comorbidity;
  • prior non‐inflammatory nasosinusal disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01513837

Locations
Spain
Sociedad Española de Neumología y Cirugía Torácica (SEPAR)
Barcelona, Catalonia, Spain, 08029
Sponsors and Collaborators
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Sociedad Española de Neumología y Cirugía Torácica
  More Information

No publications provided

Responsible Party: José Antonio Castillo Vizuete, MD, Sociedad Española de Neumología y Cirugía Torácica
ClinicalTrials.gov Identifier: NCT01513837     History of Changes
Other Study ID Numbers: SEPARALAT-1010-PII
Study First Received: January 17, 2012
Last Updated: September 7, 2012
Health Authority: Spain: Ministry of Health and Consumption

Additional relevant MeSH terms:
Asthma
Sinusitis
Bronchial Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Lung Diseases
Respiratory Hypersensitivity
 Hypersensitivity, Immediate
Hypersensitivity
Immune System Diseases
Paranasal Sinus Diseases
Nose Diseases
Respiratory Tract Infections
Otorhinolaryngologic Diseases

ClinicalTrials.gov processed this record on May 16, 2013