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Clinical Trial Summary

This is a single centre randomised, placebo-controlled phase 2 study in which 96 children age 4 to 16 years with moderate to severe, longstanding allergic eczema will be enrolled.


Clinical Trial Description

Following a 4 to 6 week period on standardised treatment (run-in period, to ensure everyone starts with the same treatment approach), participants will be randomised to an active or dummy temperature-controlled laminar airflow (TLA) device, which has been shown to markedly reduce exposure to particles which can cause allergic reactions when being inhaled (inhaled allergens) and other particles which are in the air the investigators breathe in. This has been shown to be an effective treatment of atopic asthma. The participants will undergo a 12-week treatment period. The device will then be removed and a final follow-up visit occurs at 16 weeks. The total study duration, including the run-in period is up to 22 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03795506
Study type Interventional
Source Imperial College London
Contact Sabrina Kapur
Phone +44 (0) 7776462345
Email imperial.tla4ae@nhs.net
Status Recruiting
Phase N/A
Start date July 8, 2019
Completion date May 31, 2025

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