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Efficacy and Adverse Effects of Ginger extract and loratadine for Treatment of Allergic rhinitis patients

Comparative study on Efficacy and Adverse Effects of Ginger extract and loratadine for Treatment of Allergic rhinitis patients (Clinical Trial Phase III)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20191018002
Enrollment
Unknown
Registered
2019-10-18
Start date
2019-03-01
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

Interventions

Ginger extract capsule at dose of 250 mg two times a day after meal daily for 42 days ,Loratadine tablet at dose of 10 mg one times a day after morning meal daily for 42 days
Experimental Drug,Active Comparator Drug

Sponsors

Center of Excellence on Applied Thai Traditional Medicine Research (CEATMR)
Lead Sponsor
Faculty of Medicine&#44
Collaborator
Thammasat University&#44
Collaborator
Thailand
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.. Patients have history of allergic rhinitis on the basis of “Allergic Rhinitis and its Impact on Asthma”;itching and nasal obstruction, watery nasal discharge, sneezing, congestion 2. Patients have moderate allergic rhinitis diagnosed by doctor with a minimum total nasal symptom score of 5 points 3. Volunteers wish to participate in the research

Exclusion criteria

Exclusion criteria: 1. Patients have ginger allergy. 2. Patients get serious side effects from loratadine. 3. Patients have fever. 4. Patients have respiratory disease such as tuberculosis, nasal polyps. 5. Patients have history of disease: heart disease, kidney disease, liver disease, epilepsy, high blood pressure, severe asthma and gall Stone. 6. Patients have higher than normal value in liver function and renal function. 7. Patients are pregnant or breastfeeding. 8. Immunocompromised patients 9. Patients have taken anti-coagulant, anti-platelet aggregation medications, Macrolides(erythromycin, clarithromycin), Imidazole (ketoconazole, itraconazole, fluconazole), HIV protease inhibitors, Other drugs that inhibit the enzyme CYP450 (cimetidine, metronidazole, zafirlukast, SSRIs) 10. Patients can not stop taking antihistamine or intranasal steroids for 1 week before trial. 11. Communication problems especially listening and interview. 12. The patient cannot be free from the research plan for 14 days. 13. Those who are participating in another research project.

Design outcomes

Primary

MeasureTime frame
Nasal symptom 42 days Total nasal symptom score,Nasal patency 42 days Acoustic rhinometry

Secondary

MeasureTime frame
Quality of Life 42 days Rhinoconjuctivitis Quality of Life questionnaires (Rcq-36),safety 42 days blood analysis

Countries

Thailand

Contacts

Public ContactArunporn Itharat

Center of Excellence on Applied Thai Traditional Medicine Research (CEATMR)

researchclub_herb@hotmail.com0-2926-9749

Outcome results

None listed

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