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Study on the efficacy of levocetirizine hydrochloride oral solution in the treatment of asthma and viral wheezing in young allergic children

Study on the efficacy of levocetirizine hydrochloride oral solution in the treatment of asthma and viral wheezing in young allergic children

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092021
Enrollment
Unknown
Registered
2024-11-07
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Allergic asthma and viral wheezing

Interventions

control group:Given inhaled corticosteroids, short-acting ß2 receptor agonists can be used as needed to relieve asthma and acute wheezing symptoms.
observer group:On the basis of the control group, levocetirizine hydrochloride oral solution was given once a day, 1.25 mg ( 2.5 ml ) each time.

Sponsors

West China Second Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.5 Years to 2 Years

Inclusion criteria

Inclusion criteria: 1.Age 6 months to 2 years ( including boundary age ), regardless of gender ; 2.Children with wheezing symptoms and clinical diagnosis of asthma or viral wheezing ; 3.There is a history of personal allergies, allergic diseases including atopic dermatitis, allergic rhinitis, gastrointestinal allergies, urticaria, food allergies ; 4.Specific IgE detection of allergens or skin prick test was positive ; 5.To obtain the written consent of the guardian ; 6.Can be written by the guardian of the patient diary card

Exclusion criteria

Exclusion criteria: 1.Oral glucocorticoid drugs were used within 7 days before enrollment ; 2.Oral antihistamines were used within 3 days before enrollment ; 3.Children who are allergic to the components of levocetirizine hydrochloride preparations or piperazine derivatives such as hydroxylazine, cetirizine, and cyclazine or have a history of allergy ; 4.Children with snoring and diagnosed adenoidal hypertrophy have airway structural abnormalities, congenital heart disease, bronchopulmonary dysplasia, bronchiectasis, bronchial foreign body, tuberculosis and other diseases that may affect wheezing ; 5.Children with mental illness, hematological diseases, systemic infectious diseases and malignant tumors ; 6.People who are participating in other clinical trials or have participated in other clinical trials in the past 3 months ; 7.Investigators judged that children who were not suitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Therapeutic effectiveness;

Secondary

MeasureTime frame
Wheezing symptom score;total nasal symptom score;Skin symptom score;VAS score;Use of inhaled short-acting ß2 receptor agonists;

Countries

China

Contacts

Public ContactLiu hanmin

West China Second Hospital of Sichuan University

3821302232@qq.com+86 181 8060 2219

Outcome results

None listed

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