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Clinical Efficiency and Safety of the Extract and Spores of Ganoderma lucidum in Patients with Persistent Allergic Rhinitis

Clinical Efficiency and Safety of the Extract and Spores of Ganoderma lucidum in Patients with Persistent Allergic Rhinitis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12001960
Enrollment
Unknown
Registered
2012-02-24
Start date
2012-04-02
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Allergic rhinitis

Interventions

2:fexofenadine
3:extract of Ganoderma lucidum
4:extract of Ganoderma lucidum

Sponsors

Assoc. Prof. Dr. Supanimit Teekachunhatean
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Out-patients of either sex, 18-60 years of age, suffering from persistent allergic rhinitis (PER) according to the Allergic Rhinitis and its Impact on Asthma (ARIA) World Health Organization (WHO) guideline as: duration of symptoms > 4 days/week and > 4 weeks, positive skin prick test response to 1 or more allergen. Total nasal symptom scores must be > or = 6 in the 2 previous weeks. All patients have to sign the written consent form to participate in the study.

Exclusion criteria

Exclusion criteria: Patients must not have the following diseases or conditions: structural abnormalities of the nose such as deviated nasal septum and nasal polyps, acute or chronic upper respiratory tract infection within the last 2 weeks, use of oral or topical nasal steroid within the last 4 weeks, immunotherapy within the last 1 year, nasal surgery within the last 4 weeks, history of asthma, cardiovascular diseases, uncontrolled hypertension, cancer, diabetes mellitus, benign prostatic hyperplasia, liver or kidney diseases, clinically significant abnormalities in blood chemistry and hematology, pregnancy and lactation.

Design outcomes

Primary

MeasureTime frame
Total nasal symptom score;

Countries

Thailand

Contacts

Public ContactAssoc. Prof. Dr. Supanimit Teekachunhatean
steekach@med.cmu.ac.th+66 (0) 53945353

Outcome results

None listed

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