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Qinglong Tuomin Decoction in the treatment of children with allergic rhinitis:a randomized, double-blind clinical study T

Qinglong Tuomin Decoction in the treatment of children with allergic rhinitis:a randomized, double-blind clinical study T

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072470
Enrollment
Unknown
Registered
2023-06-14
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

allergic rhinitis

Interventions

observation group:Qinglong Duomin Decoction
observation group:Levocetirizine hydrochloride placebo
control group:Levocetirizine Hydrochloride
control group:Qinglong Duomin Decoction placebo

Sponsors

Dongguan Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 14 Years

Inclusion criteria

Inclusion criteria: (1) Those who meet the diagnostic criteria of western medicine and traditional Chinese medicine for allergic rhinitis, voluntarily take the test and sign the informed consent; (2) Age: 3-14 years old, gender is not limited; (3) Those who have not used hormones, immunosuppressants and other related drugs that affect the examination and judgment of experimental results one week before inclusion in this study; (4) The patient gave informed consent and voluntarily followed up with the patient and truthfully fed back the information to the patient;

Exclusion criteria

Exclusion criteria: (1) Those who do not meet any of the inclusion criteria; (2) Those with nasal congestion and runny nose due to other reasons such as colds, nasal polyps, sinusitis, abnormal nasal structure, congenital nasal structure defects, etc.; (3) Patients with serious congenital diseases or wasting diseases of the heart, liver, kidney and nerve, hematopoietic system, or other underlying diseases that affect the judgment and treatment, or patients with mental diseases; (4) Those who are unable to insist on taking medicines and follow-up consultations as required, and who cannot cooperate with feedback information; (5) Those who are participating in clinical trials of other drugs.

Design outcomes

Primary

MeasureTime frame
TNSS;VAS;TCM Syndrome Score;

Secondary

MeasureTime frame
TNNSS;Quality of life score for children with allergic rhinitis;serum specific IgE;Nasal Acoustic Reflex Measurement;

Countries

china

Contacts

Public ContactZhang Yanhua

Dongguan Maternal and Child Health Hospital

810478316@qq.com+86 136 5049 0183

Outcome results

None listed

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