Trials / Completed
CompletedNCT02576808
Study of Efficacy and Safety of Ginger Extract Compared With Loratadine for Treatment of Allergic Rhinitis
Comparative Study of Efficacy and Adverse Effects of Ginger Extract and Loratadine for Treatment of Allergic Rhinitis Patients (Clinical Trial Phase II)
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- Thai Traditional Medical Knowledge Fund · Other Government
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
Efficacy and adverse effects of Ginger extract in treating allergic rhinitis patients compared with Loratadine.The double blind randomized controlled trial study was approved by the Human Research Ethics Committee of Thammasat University NO.1.
Detailed description
The double blind randomized controlled trial study. Patients who meet the inclusion criteria and do not fall into any exclusion criteria will be randomly placed into the experimental group, who will receive ginger extract capsules, or the control group, who will receive loratadine for 42 days.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ginger extract | Ginger extract capsule at dose of 250 mg two times a day after meal daily for 42 days |
| DRUG | Loratadine | Loratadine tablet at dose of 10 mg one times a day after morning meal daily for 42 days |
Timeline
- Start date
- 2015-10-01
- Primary completion
- 2017-10-01
- Completion
- 2017-10-01
- First posted
- 2015-10-15
- Last updated
- 2017-10-10
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT02576808. Inclusion in this directory is not an endorsement.