Prevalence and Impact of Pertussis and RSV on Asthma Severity and Control

NCT06286007 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 784

Last updated 2024-03-01

No results posted yet for this study

Summary

The main objective is to estimate the annual symptomatic incidence of Bordetella pertussis and RSV infections in patients aged 18 years and over with asthma, which will be identified by PCR, for Bordetella pertussis and by PCR for RSV performed at a specific timepoint from onset of symptoms for each symptomatic Acute Respiratory Infection (ARI).

A multicentre prospective cohort study will be undertaken in Spain. Thirty-five centres from different autonomous communities in Spain will participate in the study.

Participants will be asked to report to the investigator if they experience an asthma exacerbation or symptoms of acute respiratory infection with 2 years follow up

Conditions

  • Asthma
  • Pertussis
  • RSV Infection

Interventions

DIAGNOSTIC_TEST

PCR

Depending on the symptoms presented and date of symptom onset, for pertussis, patients will undergo a nasopharyngeal swab specimen for PCR if onset of the symptoms was within the past 3 weeks For RSV, patients will undergo a nasopharyngeal swab specimen for PCR if onset of the symptoms was within the past 72 hours.

Sponsors & Collaborators

  • Translational Research In Airway Diseases Group (TRIAD)

    collaborator UNKNOWN
  • CIBER of Respiratory Diseases CIBERES

    collaborator UNKNOWN
  • Complexo Hospitalario Universitario de A Coruña

    collaborator OTHER
  • Hospital de Galdakao

    collaborator OTHER
  • Hospital Universitario Doctor Peset

    collaborator OTHER
  • Hospital San Pedro de Alcantara

    collaborator OTHER
  • Hospital Universitario Marqués de Valdecilla

    collaborator OTHER
  • Hospital Universitario Vall d´Hebron

    collaborator UNKNOWN
  • Universitat Autonoma de Barcelona

    collaborator OTHER
  • Universidade de Santiago de Compostela

    collaborator UNKNOWN
  • Consortium for Biomedical Research in Epidemiology and Public Health

    collaborator UNKNOWN
  • Hospital Universitario Virgen del Rocio

    collaborator UNKNOWN
  • Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

    collaborator OTHER
  • University Hospital Virgen de las Nieves

    collaborator OTHER
  • Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

    collaborator OTHER
  • Germans Trias i Pujol Hospital

    collaborator OTHER
  • Hospital of Navarra

    collaborator OTHER
  • Hospital Universitario de Jerez de la Frontera

    collaborator UNKNOWN
  • Hospital El Bierzo

    collaborator OTHER
  • Hospital Clinico Universitario San Cecilio

    collaborator OTHER
  • Hospital Donostia

    collaborator OTHER
  • Hospital Universitario Central de Asturias

    collaborator OTHER
  • Hospital Universitario de la Ribera

    collaborator UNKNOWN
  • Hospital Costa del Sol

    collaborator OTHER
  • Hospital General Universitario Dr. Balmis

    collaborator UNKNOWN
  • Hospital de Sagunto

    collaborator OTHER
  • Hospital Lluis Alcanyís de Xàtiva

    collaborator UNKNOWN
  • Hospital Universitario Lucus Augusti

    collaborator OTHER
  • Hospital del Mar

    collaborator OTHER
  • Hospital Universitario Virgen de la Arrixaca

    collaborator OTHER
  • Hospital Clinic of Barcelona

    collaborator OTHER
  • Hospital Clinico Universitario de Santiago

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
99 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-21
Primary Completion
2024-07-31
Completion
2026-07-01

Countries

  • Spain

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06286007 on ClinicalTrials.gov