Role of NLRP3 Inflammasone and Hypoxia in the Severity of Osteoporosis in Patients With Bronchiectasis
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| ClinicalTrials.gov Identifier: NCT03467035 |
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Recruitment Status : Unknown
Verified March 2018 by Chun-Hua Wang, MD, Chang Gung Memorial Hospital.
Recruitment status was: Recruiting
First Posted : March 15, 2018
Last Update Posted : March 15, 2018
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| Condition or disease | Intervention/treatment |
|---|---|
| Bronchiectasis Adult Osteoporosis, Osteopenia | Other: Inflammasone |
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.
| Study Type : | Observational [Patient Registry] |
| Estimated Enrollment : | 80 participants |
| Observational Model: | Cohort |
| Time Perspective: | Prospective |
| Target Follow-Up Duration: | 1 Year |
| Official Title: | Role of NLRP3 Inflammasone and Hypoxia in the Severity of Osteoporosis in Patients With Bronchiectasis |
| Actual Study Start Date : | December 21, 2017 |
| Estimated Primary Completion Date : | December 31, 2018 |
| Estimated Study Completion Date : | June 30, 2019 |
| Group/Cohort | Intervention/treatment |
|---|---|
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desaturation
ΔSpO2 >10% or lowest SpO2<90 during baseline six minute walk test Check serum level of inflammasone, such as IL-1beta, TGF-beta TRT-PCR for PBMC |
Other: Inflammasone
Serum level of cytokine and RT-PCR for PBMC |
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non-desaturation
ΔSpO2 <10% and lowest SpO2>90 during baseline six minute walk test Check serum level of inflammasone, such as IL-1beta, TGF-beta TRT-PCR for PBMC |
Other: Inflammasone
Serum level of cytokine and RT-PCR for PBMC |
- six minute walk test [ Time Frame: 6 months ]six minute walk test distance
Biospecimen Retention: Samples With DNA
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| Ages Eligible for Study: | 20 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- willing to sign a written consent form
- Male and female subjects with bronchiectasis diagnosed by high-resolution computed tomography
- willing to accept 6-minute exercise pulmonary function test and blood draw
- Men and women over the age of 20
- Has undergone chest computed tomography and bone density examination in the recent five years
Exclusion Criteria:
- pregnant women or lactating women
- asthma, lung resection history before the screening period
- active Tuberculosis infection
- Have received oral steroid treatment within 30 days
- current acute attack or clinical symptoms instability of bronchiectasis
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03467035
| Contact: Hung-Yu Huang, MD | 033281200 ext 8470 | b9202071@cgmh.org.tw | |
| Contact: Chun-Hua Wang, MD | 033281200 ext 8468 | wchunhua@ms7.hinet.net |
| Taiwan | |
| Chang Gung Memorial Hospital | Recruiting |
| Taipei, Taiwan, 333 | |
| Contact: Hung-Yu Huang, MD 033281200 ext 8470 b9202071@cgmh.org.tw | |
| Study Director: | Chun-Hua Wang | Chang Chung Memorial Hospital |
Publications:
| Responsible Party: | Chun-Hua Wang, MD, professor, Chang Gung Memorial Hospital |
| ClinicalTrials.gov Identifier: | NCT03467035 |
| Other Study ID Numbers: |
201701317A3 |
| First Posted: | March 15, 2018 Key Record Dates |
| Last Update Posted: | March 15, 2018 |
| Last Verified: | March 2018 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Osteoporosis Bone Diseases, Metabolic Bronchiectasis Hypoxia Bone Diseases |
Musculoskeletal Diseases Metabolic Diseases Signs and Symptoms, Respiratory Bronchial Diseases Respiratory Tract Diseases |

