RECRUITINGOBSERVATIONAL
Study on Disease Progression and Nutritional Status in Bronchiectasis
A Study of the Association Between Progression and Nutritional Status in Bronchiectasis
About This Trial
Bronchiectasis is a common lung disease. The Bronchiectasis Severity Index (BSI) is a widely used assessment system. The body mass index (BMI) is a commonly used measure of nutritional status, but it has its limitations. To provide a more comprehensive assessment, the investigators also consider other nutrition-related indices such as upper arm circumference, calf circumference, skinfold thickness and grip strength. The investigators will specify the relationship between nutritional status and disease progression by measuring nutrition-related indicators and tracking participants' disease progression.
Who May Be Eligible (Plain English)
Who May Qualify:
- Age ≥18 years
- Participants' pulmonary imaging findings and clinical presentation met the diagnostic criteria for bronchiectasis
- willing to sign a consent form was signed
Who Should NOT Join This Trial:
- 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 willing to sign a consent form or who refuse to participate in the clinical study
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
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
Treatments Being Tested
OTHER
inapplicable
inapplicable
Locations (2)
Wuhan Union Hospital
Wuhan, Hubei, China
Wuhan Union Hospital,China
Wuhan, Hubei, China