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Withdraw. Bacterial lysates are allergic to children A preliminary study on the curative effect and treatment mechanism of rhinitis

Bacterial lysates are allergic to children A preliminary study on the curative effect and treatment mechanism of rhinitis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052864
Enrollment
Unknown
Registered
2021-11-06
Start date
2021-11-14
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Allergic rhinitis

Interventions

Group B:Nasal cavity irrigation and conventional treatment
Group C:Nasal cavity flushing, conventional treatment and Panfuxu

Sponsors

Children's Hospital Affiliated to Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 3 years, and 5 times/year; 5. The volume of adenoids accounts for <= 70% of the nasopharynx; 6. Have not used anti-allergic drugs such as glucocorticoids, antihistamines, leukotriene receptor antagonists in the past 2 weeks; 7. The children and their guardians have good compliance. The subjects of the experimental group need to be willing to receive Panfuxu treatment, be able to cooperate with the drug treatment for 1 to 3 months, voluntarily participate in this clinical study and sign an informed consent.

Exclusion criteria

Exclusion criteria: 1. Have had nasal surgery, nasal deformities, etc.; 2. With nasal polyps, asthma, nasal septum deviation and other causes of nasal congestion; 3. Acute upper respiratory tract infection in the past 2 weeks; 4. Related metabolic disorders, cardiovascular diseases, nervous system diseases, blood system diseases, gastrointestinal diseases, cerebrovascular diseases and respiratory diseases, etc.; 5. Subjects with severe liver and kidney dysfunction and allergies; 6. Subjects deemed unsuitable by other researchers to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Symptom score;Serum immunoglobulin total IgE, IgA, IgG, IgM;Number and percentage of eosinophils;Lymphocytes CD3, CD16, CD56, CD19, CD8, CD4;Cytokines IL2, IL4, IL6, IL10, TNF, INF-r levels;

Countries

China

Contacts

Public ContactFu Yong

Children's Hospital Affiliated to Zhejiang University School of Medicine

fyent@163.com+86 15888828299

Outcome results

None listed

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