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Bronchiectasis Adult clinical trials

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NCT ID: NCT03643302 Completed - Clinical trials for Bronchiectasis Adult

Airway Clearance and Bronchoalveolar Lavage for Bronchiectasis Patients With Exacerbation

Start date: February 1, 2018
Phase:
Study type: Observational

No study have evaluated the efficacy and safety of airway clearance therapy (ACT) and bronchoalveolar lavage (BAL) under bronchoscope for bronchiectasis. This study aimed to evaluate the clinical efficacy and safety of tran-bronchoscopy airway clearance and bronchoalveolar lavage in the treatment of moderate to severe bronchiectasis with acute exacerbation:A randomized, prospective cohort study.

NCT ID: NCT03467035 Recruiting - Clinical trials for Bronchiectasis Adult

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

Start date: December 21, 2017
Phase: N/A
Study type: Observational [Patient Registry]

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.

NCT ID: NCT03383939 Completed - Clinical trials for Bronchiectasis Adult

Inhaled A1AT in Adult Stable Bronchiectasis

Start date: June 1, 1996
Phase: N/A
Study type: Interventional

Aim: to investigate the influence of alpha1-antitrypsin (A1-AT) nebulization on levels of A1-AT in BAL and plasma in patients with stable bronchiectasis. Method: single-blind placebo-controlled randomised clinical trial. 19 stable bronchiectasis patients with chronic bronchial infection and 10 control patients (without bronchiectasis) underwent a bronchoscopy in order to assess levels and inhibitory capacity of A1AT and neutrophilic elastase. Afterwards, the 19 bronchiectasis patients were randomly allocated to receive inhaled A1AT 250mg diluted in 10ml 0.9% saline solution once a day for a month (Group A, n: 10) or placebo (10ml 0.9% saline solution; group B, n: 9). A new BAL was performed in both groups (A and B) 24 hours after the end of treatment (1month) to re-analyze A1AT and NE.

NCT ID: NCT03177889 Not yet recruiting - Quality of Life Clinical Trials

Lung Dispersing, Turbid Descending and Gut Clearing Decoction for Bronchiectasis

LUNG-CLEAR
Start date: December 31, 2021
Phase: N/A
Study type: Interventional

Bronchiectasis is a chronic airway disease which confers significant healthcare burden, with limited therapeutic approaches. From the perspective of traditional Chinese medicine, congenital insufficiency of the lung, spleen and kidney, when coupled with external injury or mood impairment, may collectively contribute to bronchiectasis pathogenesis due to heat trapping in the phlems, congestion of wind evils and stagnation of blood. Here, the investigators will explore the Lung Dispersing, Turbid Descending and Gut Clearing Decoction (LTGD) which targets at expelling the wind evil in patients with bronchiectasis. The investigators sought to conduct a multicenter, randomized cross-over trial which investigates the efficacy and safety of LTGD on clinically stable bronchiectasis.

NCT ID: NCT03125174 Completed - Clinical trials for Bronchiectasis Adult

Characterization of Airway Mucus in Bronchiectasis Patients and Healthy Controls

Start date: March 10, 2017
Phase: N/A
Study type: Observational

Analysis of mucus, mucin and DNA concentration, MUC5B/5AC ratio, rheology, osmotic pressure, cohesion and nucleotides in sputum on 30 individual samples of good quality in healthy individuals and those with bronchiectasis. (60 total)