Recruiting

Observational Study

Sponsor:

University of British Columbia

Code:

NCT03937427

Conditions

Chronic Rhinosinusitis (Diagnosis)

Asthma

Eligibility Criteria

Sex: All

Age: 19+

Healthy Volunteers: Not accepted

Study Details

Brief summary:

Chronic rhinosinusitis (CRS) impacts approximately 5% of Canadians. CRS patients suffer from a combination of symptoms that include facial pain, nasal obstruction, hyposmia and mucopurulence discharge. Asthma may additionally worsen quality of life and many patients suffer from both conditions. The unified airway model illustrates a link between both conditions as tissue from the middle ear to the sinus cavity to the lungs function as one unit. Despite evidence for the unified airway model in the setting of CRS and asthma, there are no studies to our knowledge that have evaluated the microbiome (the resident microbes and their genetic expressions that affect disease) of the upper and lower airways in this patient population. Determining the microbiome of the upper and lower airways in patients suffering from CRS and asthma will further support the unified airway model but more importantly, will help contribute to understanding the pathophysiology of this inflammatory process and may help guide future management.

Conditions

Chronic Rhinosinusitis (Diagnosis)

Asthma

Study ID

NCT03937427

Start date

Jan 16, 2017

Status verified date

May, 2019

Completion date

Apr, 2020

Anticipated

Primary completion date

Dec, 2019

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 19+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 19 years or older
  • Able to speak and understand English
  • Diagnosed with chronic rhinosinusitis with or without asthma and COPD or with a sinonasal tumor
  • Undergoing sinus surgery in St Paul's Hospital

Exclusion Criteria:

  • Oral antibiotics in the past month prior to surgery;
  • Immunocompromised;
  • Prior lung transplants;
  • Known sinonasal or bronchial tumors, current or previous;
  • Smoking;
  • Known bleeding disorders:
  • Deemed unfit by the rhinologists/respirologist for bronchoscopy.

Study Design

Enrollment

24 participants

Anticipated

Interventions and Outcome Measures

Arms

CRS with Asthma

CRS without Asthma

Primary outcome measure

  • Pathology (histological assessment) [ Time Frame: 1 day ]
  • Gene Expression Patterns [ Time Frame: 1 day ]

Central Contacts and Locations

Central contacts

Locations

St. Paul's Hospital

Recruiting

Vancouver, B.C., Canada, V6Z 1Y6

Contacts

More Information

Sponsor

University of British Columbia

Last update posted

May 3, 2019

Last verified

May, 2019

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of British Columbia on 2019-05-03.