RecruitingNCT05604495

Screening for Cystic Fibrosis and Cystic Fibrosis Related Disorders in Chinese Adults With Bronchiectasis

The Clinical and Genetic Characteristics of Cystic Fibrosis and Cystic Fibrosis Disorders in Chinese Adults With Bronchiectasis


Sponsor

Shanghai Pulmonary Hospital, Shanghai, China

Enrollment

1,000 participants

Start Date

Sep 7, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

The study carries out Sweet Tests and CFTR-mutation screening to explore the prevalence, clinical characteristics, and prognosis of cystic fibrosis, as well as the CFTR-mutation spectrum in Chinese adults with bronchiectasis. The study is multi-centered, prospective, non-interventional, and observational.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Age>18 years, the diagnosis of bronchiectasis needs a reference to the definition of "non-cystic fibrosis bronchiectasis guideline" published by the British Thoracic Society in 2017 or 2021 China bronchiectasis expert consensus, clinical symptoms of cough and expectoration, with or without intermittent hemoptysis, and chest CT showed bronchiectasis
  • Patients who are willing to sign the consent form and participate in the study.

Exclusion Criteria8

  • Patients with incomplete essential information, which is needed for the integrity of data analysis. Essential information includes CT images, respiratory sample cultures, spirometry, and exacerbation history for at least one year.
  • Patients under 18 years old.
  • Patients with an implanted device, such as a defibrillator, neurostimulator, pacemaker, or ECG monitor.
  • Patients with a history of epilepsy or seizures.
  • Patients who are pregnant.
  • Patients that have a known sensitivity or allergy to any ingredient.
  • Over-damaged, denuded skin or other recent scar tissue.
  • Patients with Cardiac Conditions or with suspected heart problems.

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Interventions

DIAGNOSTIC_TESTSweat Test

In people with cystic fibrosis (CF), there is a problem in the transport of chloride across cell membranes. This results in higher concentrations of chloride (as salt) in sweat compared to those who do not have cystic fibrosis. So, if there is a family history or a possibility of CF, the sweat test is part of the special tests to help make, or exclude, a diagnosis of cystic fibrosis.


Locations(1)

Shanghai pulmonary hospital

Shanghai, Shanghai Municipality, China

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NCT05604495