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Clinical Trial Summary

Evaluation of the efficacy and safety of SLIT with LAIS® Mites Sublingual tablets compared to standard drug treatment in patients aged over 60 years suffering from house dust mite (HDM) induced allergic rhino-conjunctivitis with/without asthma.


Clinical Trial Description

The Total combined score (TCS), taking into account the rhinoconjunctivitis total symptom score (RTSS) and the total rescue medication score (RTMS), in the maximum expected mites exposition period (V4-V5) For the RTSS and the RTMS, the daily values as determined by the patients in their diary card are collected during the observation period over 30 days. Then, the mean daily scores during that period are calculated for both parameters. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02277483
Study type Interventional
Source Ajou University School of Medicine
Contact yun-kyoung kim, Nr
Phone 82-31-219-4467
Email forsake326@gmail.com
Status Recruiting
Phase Phase 4
Start date October 2014
Completion date December 2016

See also
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Completed NCT01285830 - Primary Prevention of Allergic Disease in Early Child by Lactobacillus Reuteri Phase 2