Trials / Unknown
UnknownNCT03009136
Efficacy and Safety of So-Cheong-Ryong-Tang on Perennial Allergic Rhinitis
Efficacy and Safety of So-Cheong-Ryong-Tang on Perennial Allergic Rhinitis: Study Protocol for a Double-blind, Randomized, Parallel-group, Multi-center Trial
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 154 (estimated)
- Sponsor
- Kyung Hee University Hospital at Gangdong · Academic / Other
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to investigate the short and long term efficacy and the safety of SCRT treatment for PAR
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | SCRT | composed of eight herbs: Glycyrrhiza uralensis Fischer 1g Zingiber officinale Roscoe 0.5g Cinnamomum cassia Blume 0.2g, Ephedra sinica Stapf 0.5g, Pinellia ternata Breitenbach 2.67g, Paeonia lactiflora PALL 1g, Asiasarum sieboldi F. Maekawa 0.5g, Schisandra chinensis 2.67g (per 9g of granules) |
| DRUG | Placebos | is made of lactose, corn starch and caramel coloring, and has appearance, shape, weight, taste, and color similar to SCRT |
Timeline
- Start date
- 2016-12-31
- Primary completion
- 2018-12-01
- Completion
- 2018-12-01
- First posted
- 2017-01-04
- Last updated
- 2017-03-14
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03009136. Inclusion in this directory is not an endorsement.