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A multicenter, randomized controlled trial for interferon alpha 1b in the treatment of children with virus-induced asthmatic disease

A multicenter, randomized controlled trial for interferon alpha 1b in the treatment of children with virus-induced asthmatic disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000028749
Enrollment
Unknown
Registered
2020-01-02
Start date
2020-02-10
Completion date
Unknown
Last updated
2020-01-06

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

Conditions

Asthmatic disease

Interventions

Control group:Conventional treatment
Experimental group:Conventional treatment + nebulized IFN-a1b

Sponsors

Children's Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.5 Years to 5 Years

Inclusion criteria

Inclusion criteria: 1. aged 0.5-5 years old; 2. acute infection, clinical symptoms: fever, wheezing, cough, lung rales, wheezing, etc 3. lower respiratory tract infection caused by viru(clinical diagnosis was associated with respiratory viral infection, nasopharyngeal secretions of etiology detection of respiratory syncytial virus (RSV), adenovirus (ADV), influenza virus type A (IVA), type B (IVB), parainfluenza I type (PIV I), II (PIV II) and III (PIV III), at least one was positive); 4. Onset time<=96 hours; 5. IVIG and other biological and chemical immunoregulatory agents and antiviral agents were not used in the first week of treatment; 6. Willing and able to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergic history of interferonor contraindication to interferon; 2. severe wheezing with respiratory failure and serious complications; 3. With bronchopulmonary dysplasia, congenital airway dysplasia, bronchiectasis, bronchial foreign body, lobar pneumonia and tuberculosis; 4. WBC 12*10^9/L,classification of neutrophils significantly increased; 5. history of epilepsy or other central nervous system diseases; 6. other serious diseases, such as severe malnutrition, serious liver and kidney function damage, active peptic ulcer disease, fracture, adrenal hyperfunction, diabetes, cardio-cerebrovascular, tuberculosis, chronic obstructive pneumonia, mental disease, etc.; 7. Unable to cooperate with the study; 8. Those subjects are not suitable for this study by investigator's judgement.

Design outcomes

Primary

MeasureTime frame
Alleviate clinical symptoms;Clinical curative effect;

Secondary

MeasureTime frame
Hospitalization time;Biochemical index detection;frequency and incidence of recurrence;

Countries

China

Contacts

Public ContactZhou Fu
2382447745@qq.com+86 023 63664659

Outcome results

None listed

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