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Withdraw. Myrtle oil compound spray in children with allergic rhinitis observation and evaluation of clinical efficacy

Myrtle oil compound spray in children with allergic rhinitis observation and evaluation of clinical efficacy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052863
Enrollment
Unknown
Registered
2021-11-06
Start date
2021-11-21
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 irrigation and Biroph
Group C:Nasal cavity irrigation and conventional treatment
Group D:Nasal cavity irrigation, conventional treatment and Biroph

Sponsors

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

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 3 years, and < 18 years, no gender limit; 2. Meet the diagnostic criteria of the 2010 Guidelines for the Diagnosis and Treatment of Allergic Rhinitis in Children; 3. The course of allergic rhinitis is more than half a year; 4. The volume of adenoids accounts for <= 70% of the nasopharynx; 5. Have not used anti-allergic drugs such as glucocorticoids, antihistamines, leukotriene receptor antagonists in the past 2 weeks; 6. The children and their guardians have good compliance, can cooperate with drug treatment for 1 to 3 months, voluntarily participate in this clinical study and sign the 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;

Secondary

MeasureTime frame
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