Actively Recruiting

Age: 18Years - 85Years
All Genders
NCT06900062

The C-BRIDGE Study: China Bronchiectasis Research Involving Databases, Genomics, and Endotyping

Led by Shanghai Pulmonary Hospital, Shanghai, China · Updated on 2025-11-25

1500

Participants Needed

9

Research Sites

199 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Bronchiectasis is a heterogeneous airway disease with diverse causes, making precise diagnosis, prognosis, and treatment response prediction challenging. Identifying patient subgroups (phenotypes) and molecular profiles (endotypes) can enhance individualized assessment and management. While prior studies, primarily in European populations, have identified key phenotypes and endotypes, their relevance to Chinese patients remains unclear due to geographic and clinical differences. Specific causes of bronchiectasis, such as allergic bronchopulmonary aspergillosis (ABPA) and primary ciliary dyskinesia (PCD), may also exhibit distinct pathophysiology requiring further exploration. The C-BRIDGE Study seeks to characterize phenotypes and endotypes in Chinese bronchiectasis patients during stable disease and exacerbations, evaluate differences in clinical outcomes across these subgroups, and develop personalized medicine strategies based on these findings, applicable in China and globally. Primary Objective: To identify molecular endotypes of bronchiectasis that accurately predict prognosis and guide treatment responses. Secondary Objectives: To characterize molecular endotypes of stable bronchiectasis in Chinese patients. To define molecular endotypes of bronchiectasis exacerbations in Chinese patients. To investigate molecular endotypes specific to allergic bronchopulmonary aspergillosis (ABPA). To explore genotypes and inflammatory endotypes of cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) in Chinese patients. To validate candidate biomarkers for stable and exacerbation endotypes to support stratified medicine. To conduct in vivo or in vitro proof-of-concept studies using phenotypic data to identify patient subgroups likely to benefit from specific pharmacological interventions. Study Design: This observational cohort study will link identified patient subgroups with meaningful clinical outcomes to inform prognosis and optimize treatment strategies.

CONDITIONS

Official Title

The C-BRIDGE Study: China Bronchiectasis Research Involving Databases, Genomics, and Endotyping

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • A prior CT scan confirming bronchiectasis, accompanied by a compatible clinical syndrome including cough, sputum production, and/or recurrent respiratory tract infections.
  • Clinically stable for 4 weeks at screening, with no antibiotic or corticosteroid treatment for a pulmonary exacerbation in the preceding 4 weeks.
  • Aged between 18 and 85 years.
  • Ability to provide informed consent.
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent.
  • Age under 18 years.
  • Active tuberculosis infection.
  • Use of antibiotics or corticosteroids for a pulmonary exacerbation within the past 4 weeks.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 9 locations

1

Lin Liu

Guiyang, Guizhou, China

Actively Recruiting

2

Lei Song

Changchun, Jilin, China

Actively Recruiting

3

Qian Qi

Jinan, Shangdong, China

Actively Recruiting

4

He-feng Chen

Shanghai, Shanghai Municipality, China, 200433

Actively Recruiting

5

Zhou-fang Mei

Shanghai, Shanghai Municipality, China, 200433

Actively Recruiting

6

Jun She

Shanghai, Shanghai Municipality, China, 200437

Actively Recruiting

7

Xue-ling Wu

Shanghai, Shanghai Municipality, China, 200437

Actively Recruiting

8

Yong-hua Gao

Shanghai, Shanghai Municipality, China, 200437

Actively Recruiting

9

Xiao-long Ma

Jiaxing, Zhejiang, China

Actively Recruiting

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Research Team

Y

Yong-hua Gao, Ph.D.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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