Skip to content

The effect of azithromycin on neutrophilic asthma

The effect of azithromycin on neutrophilic asthma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003679
Enrollment
Unknown
Registered
2013-05-29
Start date
2013-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Asthma

Interventions

azithromycin group:receive azithromycin

Sponsors

Institute of Respiratory Diseases, the Second Affiliated Hospital of Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Screening criteria: 1.Informed consent; 2. between the ages of 18 and 75 years of age , including 18 and 75; 3. have recurrent episodes of wheezing , shortness of breath , chest tightness or cough and other symptoms; 4. Asthma diagnosed more than 3 months by bronchodilation test or challenge test positive; 5. ACT score 65%, Eos 65%, Eos <3%; 2. Screening period, showing good compliance, with the completion of the study are expected to be.

Exclusion criteria

Exclusion criteria: Screening criteria: 1. Regular ICS therapy is being used (regular is defined as: the use of time greater than one month and medication compliance > 80%); 2. Systemic hormone therapy or unknown oral asthma medications being regular used; 3. Respiratory infection; 4.moderate and moderate to severe acute exacerbation; 5. Allergy to macrolide antibiotics or placebo; 6. can not stop ergot derivatives, rifabutin, propylthiouracil, non-steroidal anti-inflammatory drugs, phenytoin, card carbamazepine during treatment; 7. combined with other lung diseases such as COPD, bronchiectasis, lung cancer; 8. existence of serious complications; 9. other unsuitable participate in the trial of the case (such as pregnancy, breast-feeding, do not have the legal capacity etc.). Random criteria: 1. Signs of respiratory infection during screening period; 2. Imaging, laboratory results of visit one suggest that respiratory tract infection or clinically significant abnormalities; 3.moderate and moderate exacerbations during screening period; 4. oral or intravenous use of systemic hormone therapy during screening period; 5. within (whichever is longer) 5 plasma half-life from random used antibiotic treatment or other study drug; 6. allergic for basic treatment.

Design outcomes

Primary

MeasureTime frame
interleukin-17;interleukin-1ß;interleukin-6;

Secondary

MeasureTime frame
interleukin-23;CRP;induced sputum cytology;Forced expiratory volume in one second %predicted;Asthma control test;Peripheral blood leukocyte count;interleukin-8;Neutrophil elastase;

Countries

China

Contacts

Public ContactChangzheng Wang

Institute of Respiratory Diseases, the Second Affiliated Hospital of Third Military Medical University. Chongqing

czwang@netease.com+86 13983815706

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026