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Role of NLRP3 Inflammasone and Hypoxia in the Severity of Osteoporosis in Patients With Bronchiectasis

Role of NLRP3 Inflammasone and Hypoxia in the Severity of Osteoporosis in Patients With Bronchiectasis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03467035
Enrollment
80
Registered
2018-03-15
Start date
2017-12-21
Completion date
2019-06-30
Last updated
2018-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiectasis Adult, Osteoporosis, Osteopenia

Brief summary

The objectives of this research grant are to determine the association of hypoxia with the severity of osteoporosis in the patients with bronchiectasis and whether the mechanism of inflammation is triggered by inflammasones, which makes it more prone to osteoporosis in patients with bronchiectasis.

Detailed description

80 patients with proven bronchiectasis, diagnosed by high-resolution computed tomography (HRCT), will be recruited from our outpatient clinic of Chang Gung Memorial Hospital with written informed consent. Inclusion criteria are: daily sputum \> 10 ml; absence of asthma or other unstable systemic diseases; and steady-state bronchiectasis (\< 10% alteration of 24 h sputum volume, FEV1, and FVC, and in the absence of deterioration in respiratory symptoms at baseline visits). Exclusion criteria include: unreliable clinic attendance; regular user of inhaled or oral corticosteroids; history of lung resection and known asthma defined according to American Thoracic Society guidelines. The lung function and desaturation will be assessed by six-minute walking tests and the severity of disease will be evaluated by HRCT scores. Peripheral blood sample (40ml/person) is performed to analyze the bone turnover markers and the level of Hif in PBMC.

Interventions

OTHERInflammasone

Serum level of cytokine and RT-PCR for PBMC

Sponsors

Chun-Hua Wang, MD
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. willing to sign a written consent form 2. Male and female subjects with bronchiectasis diagnosed by high-resolution computed tomography 3. willing to accept 6-minute exercise pulmonary function test and blood draw 4. Men and women over the age of 20 5. Has undergone chest computed tomography and bone density examination in the recent five years

Exclusion criteria

1. pregnant women or lactating women 2. asthma, lung resection history before the screening period 3. active Tuberculosis infection 4. Have received oral steroid treatment within 30 days 5. current acute attack or clinical symptoms instability of bronchiectasis

Design outcomes

Primary

MeasureTime frameDescription
six minute walk test6 monthssix minute walk test distance

Countries

Taiwan

Contacts

Primary ContactHung-Yu Huang, MD
b9202071@cgmh.org.tw033281200
Backup ContactChun-Hua Wang, MD
wchunhua@ms7.hinet.net033281200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026