Skip to content

Effectiveness and safety of Thai traditional medicine (Yaprabchombhutaweeb) on allergic rhinitis

Effectiveness and safety of Thai traditional medicine (Yaprabchombhutaweeb) on allergic rhinitis: A randomized controlled trial.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180906003
Enrollment
300
Registered
2018-09-06
Start date
2018-09-10
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 Yaprabchombhutaweeb&#44

Interventions

Yaprabchombhutaweeb 450 mg/capsule (Mixed herbal formulation),Loratadine 10 mg/tablet
Experimental Drug,Active Comparator Drug
Yaprabchombhutaweeb,Loratadine

Sponsors

Agricultural Research Development Agency (Public Organization)
Lead Sponsor
None,None
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Male or female with age 18-60 years 2. Patients that diagnosed allergic rhinitis or 3. Patients who had a history of allergic cause and one or more of the following symptoms: nasal congestion, runny nose, itchy nose, or sneezing and 4. Patients who presented watery rhinorrhea or runny nose with one or more of the following symptoms: nasal congestion, itchy nose, sneezing, itchy watery eye

Exclusion criteria

Exclusion criteria: 1. Patients with complication of allergic rhinitis such as rhinosinusitis or upper respiratory tract infection, fever (body temperature > 38.5 oC ) 2. Patients with abnormal nasal structure and needed current medication such as Nasal Polyp 3. Patients with allergic rhinitis requiring topical or oral medications containing anti-histamine drug within 7 days before starting date of study 4. Patients who requiring medications that interfere with Yaprabchomphutaweeb or loratadine such as phenytoin, propranolol, rifampicin 5. Patients with other conditions that would interfere with the assessments such as uncontrolled COPD 6. Patients who present symptom of peptic ulcer or GERD 7. Pregnant women 8. Nursing or breast feeding women 9. Patients with renal impairment or abnormal of liver enzyme 10. The drinker or smoker

Design outcomes

Primary

MeasureTime frame
Success rate (no symptoms or TNSS-4 score improve > 80%), improvement rate (TNSS-4 score improve >50 At week 4 Total nasal symptom scores -4 scale (TNSS-4) questionnaire assessed by physician

Secondary

MeasureTime frame
The difference of Total nasal symptom scores 4 scale, quality of life score, ADRs, AEs, time to cure At week 1, 2, 4 TNSS-4, Rcq-36 questionnaire (QOL of chronic allergic rhinitis patient), ADR, AEs

Countries

Thailand

Contacts

Public ContactRatree Sawangjit

Faculty of Pharmacy, Mahasarakham University

ratree.m@msu.ac.th043754360

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026