Macrolide Mediates Pulmonary Infection of Pseudomonas Aeruginosa

NCT ID: NCT02491723

Last Updated: 2016-10-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 71 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-01-31
• Study Completion Date: 2016-01-31

Brief Summary

It is acknowledged that IL-18, as a product of the inflammasome, is involved in host defence against viral and bacterial stimuli by modulating the immune response. The aim of this study was to determine IL-18 levels in serum of patients with Bronchiectasis and to investigate whether macrolide attenuate its levels.

Detailed Description

Non-cystic fibrosis bronchiectasis is a respiratory disease characterized by persistent airway inflammation and dilation of bronchial wall driven by various causes. Patients with bronchiectasis suffer from excessive sputum production, recurrent exacerbations, and progressive airway destruction. It was reported that 30%-40% patients were infected with Pseudomonas aeruginosa. Major therapy for bronchiectasis is focused on breaking the "vicious cycle" of mucus stasis, infection, inflammation, and airway destruction. Currently a number of clinical trials have showed that macrolide effectively used in the treatment of non-CF bronchiectasis. Evidence has indicated that 14- and 15-membered ring macrolides possess immunomodulation and anti-inflammatory functions beyond their antimicrobial properties. However, the underlying mechanisms that account for the anti-inflammatory actions of macrolides have not yet to be elucidated, and the activities do not appear to be controlled by a single mechanism.Interleukin-18 (IL-18), along with interleukin-1b (IL-1b), is produced by inflammasomes when activated by a number of pathogen, environmental or host-derived danger signals. Inflammasomes are innate immune regulatory protein complexes which seem to play a key role in the host immune response of patients with Bronchiectasis. The aim of this study was to determine IL-18 levels in serum of patients with Bronchiectasis and to investigate whether macrolide could attenuate its levels.

Conditions

Bronchiectasis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Azithromycin group

Patients with non-cystic bronchiectasis were treated with azithromycin. The intervention was 500mg daily for three to five days.

Group Type: EXPERIMENTAL

Azithromycin

Intervention Type: DRUG

Patients with bronchiectasis treated with Azithromycin for three to five days.

Interventions

Azithromycin

Patients with bronchiectasis treated with Azithromycin for three to five days.

Intervention Type: DRUG

Other Intervention Names

macrolide

Eligibility Criteria

Inclusion Criteria

1. Able to provide written informed consent.

2. Confirmed diagnosis of bronchiectasis by HRCT.

3. Aged 18-85 years.

Exclusion Criteria

1. Bronchiectasis as a result of CF or active tuberculosis or non-tuberculous mycobacterial (NTM) infection.

2. Allergy to macrolide antibiotics

3. Any history of severe cardiopulmonary dysfunction, eg. left heart failure, Unstable cardiac arrhythmias

4. pregnant or nursing

5. hypogammaglobulinemia or other autoimmune disease 6. diagnosed with ABPA

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Jin-Fu Xu

OTHER

Sponsor Role: lead

Responsible Party

Jin-Fu Xu

deputy director

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Jin-Fu Xu, PhD

Role: STUDY_DIRECTOR

Shanghai Pulmonary Hospital, Shanghai, China

Locations

Shanghai Pulmonary Hospital

Shanghai, Shanghai Municipality, China

Countries

China

Other Identifiers

20150619

Identifier Type: -

Identifier Source: org_study_id