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The clinical study of herbal A-Pai-Sa-Li remedy for the treatment of allergic rhinitis and upper respiratory tract

The clinical study of A-Pai-Sa-Li remedy for the treatment of allergic rhinitis and upper respiratory tract

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260202007
Enrollment
60
Registered
2026-02-02
Start date
2026-08-03
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

allergic rhinitis A-Pai-Sa-li herbal remedy, Allergic rhinitis

Interventions

A-Pai-Sa-Li herbal remedy, 500 mg per capsule, 4 capsules twice daily before breakfast and dinner for 30 days.,Placebo capsules, 500 mg, 4 capsules twice daily before breakfast and dinner for 30 days
Experimental Drug,Placebo Comparator Drug
A-Pai-Sa-Li herbal remedy,Placebo

Sponsors

Thai traditional medicine knowledge fund
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male or female, aged 20-70 years. 2. Diagnosed with moderate-severe upper respiratory tract allergic disease according to the ARIA guideline 3. Pre-project blood test results as follows: eGFR more than60 mL/min AST, ALT less than 3 times the upper range Hb more than 10 g/dL 4. Women of reproductive age must have a negative urine pregnancy test. 5. Willing and willing to participate in the project and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with liver and kidney disorders 2. Patients with cardiovascular disease, taking anticoagulants, or anticoagulants, such as warfarin or aspirin 3. Patients with upper respiratory disease or who have undergone previous procedures 4. Patients with a history of herbal allergy or who have used other herbs within the past 2 weeks 5. Patients who have consumed alcohol within the month prior to and during the project 6. Patients with a history of drug use 7. Pregnant and breastfeeding women 8. Participants in other research projects

Design outcomes

Primary

MeasureTime frame
Change in total nasal symptom score Baseline, Day 14, Day 30 The nasal symptom record form.,Change in mean daily nasal symptom score Baseline, Day 14, Day 30 The daily nasal symptom diary.

Secondary

MeasureTime frame
Quality of life at 14 days and 30 day after start treatment Rhinoconjunctivitis Quality of Life Questionnaire (RCQ-36),Safety outcome From baseline to end of treatment. Number of adverse event, liver and kidney function tests (AST, ALT, eGFR)

Countries

Thailand

Contacts

Public Contactsurasak imiam

phrapokklao hospital

surasak.alexx@gmail.com039319666

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026