Clinical trial Recruiting at 1 site Observational Ages 18 to 100

Disease progression and nutritional status in bronchiectasis

Official title: A Study of the Association Between Progression and Nutritional Status in Bronchiectasis

Run by Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · NCT06344000 · Data updated 2026-11-12

The study will see if detailed nutritional measures (BMI, arm and calf circumference, skinfold thickness, and grip strength) relate to disease progression in adults with non-cystic fibrosis bronchiectasis.

Quick facts

Study typeObservational
Ages18 Years to 100 Years
SexAll
Enrollment300 (estimated)
SponsorUnion Hospital, Tongji Medical College, Huazhong University of Science and Technology
Academic / other
Locations2 sites (Wuhan, Hubei and 1 other locations)
StatusRecruiting
StartedApril 15, 2024
Main results expectedApril 15, 2027
Study endsApril 15, 2027
Registry record updatedSeptember 25, 2025
Trial IDNCT06344000 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older with imaging-confirmed non-cystic fibrosis bronchiectasis who can provide informed consent and attend study visits are ideal candidates.

Probably not a fit

Patients with cystic fibrosis, prior lung transplant, serious nonpulmonary organ failure, pregnant or lactating women, or those unable to cooperate with assessments are unlikely to benefit from this observational protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational cohort will enroll adults with non-cystic fibrosis bronchiectasis confirmed by imaging and obtain multiple nutrition-related measurements including BMI, upper arm and calf circumference, skinfold thickness, and grip strength. Investigators will record Bronchiectasis Severity Index components, clinical events such as exacerbations and hospitalizations, lung function, and microbial colonization over follow-up to track disease progression. The analysis will examine relationships between baseline and change-in nutritional indices and subsequent clinical outcomes. Participants with major organ failure, cystic fibrosis, prior lung transplant, pregnancy, or inability to consent are excluded.

Why it matters

Potential benefit: If successful, the findings could help identify patients at risk of worsening disease so clinicians can target nutritional monitoring or interventions earlier.

How similar studies have gone: Prior studies have linked low BMI and reduced fat-free mass to worse outcomes and more hospitalizations in bronchiectasis and COPD, but comprehensive multi-measure nutritional profiling in bronchiectasis remains relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥18 years
* Participants' pulmonary imaging findings and clinical presentation met the diagnostic criteria for bronchiectasis
* Informed consent was signed

Exclusion Criteria:

* Age \<18 years
* Does not meet the diagnostic criteria for bronchiectasis
* Participants with cystic fibrosis or previous lung transplantation
* Participants who are unable to cooperate with the study due to dysfunction of vital systems such as heart, brain, liver, and kidneys, or who are unable to participate in the study due to comorbid serious diseases
* Pregnant or lactating females
* Who are not able to provide informed consent or who refuse to participate in the clinical study

Where it's running

  • Wuhan Union Hospital,China
    Wuhan, Hubei, China
    Recruiting
  • Wuhan Union Hospital
    Wuhan, Hubei, China
    Not yet recruiting

Study contacts

  • Principal investigator: Xiaorong Wang — Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
  • Study coordinator: Xiaorong Wang
  • Email: rong-100@163.com
  • Phone: 18627195231

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.