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Clinical Trial Summary

The aim of this study is to investigate the efficacy and safety of Tian Jiu in the treatment of allergic rhinitis compared with placebo and waitlist patients in Hong Kong.


Clinical Trial Description

This will be a prospective, randomized, single-blinded, controlled trial in patients with AR. After a one-week run-in period, eligible subjects will be randomly assigned to the Tian Jiu group, placebo-control group and waitlist-control group. The TJ and placebo-control groups will undergo a 4-week treatment with one session per week and one 4-week post-treatment follow-up. Participants in the waitlist-control group will not receive any treatment during the first 4 weeks but will be required to be assessed. The total study period will be nine weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02470845
Study type Interventional
Source Hong Kong Baptist University
Contact
Status Completed
Phase N/A
Start date July 2014
Completion date September 2016

See also
  Status Clinical Trial Phase
Completed NCT01371786 - A Phase 1 Scintigraphy Study to Assess Nasal Deposition of Ciclesonide. Using a Novel Nasal Metered Dose Inhaler Phase 1