Upper Airway, Irritation Inflammation, Discomfort Clinical Trial
Official title:
Does House Dust From Water Damaged Buildings Cause Stronger Responses Among Occupants Than Dust From Buildings Without Water Damage? Can Occupants’ Sensitivity be Predicted by Biomarkers?
The study is focussed on two main questions:
1. The importance of dampness of the building and home dust as a factor of the subjects=
responses.
2. Can measures used in KLINIR predict the subjects’ responses to the dust?
This study therefore was arranged to test the following hypotheses:
1. Does dust in general cause inflammatory/body perceptions through e.g. an irritation
symptoms index.
2. Does the dust include effective odorants which affects an IAQ index?
3. Does dampness increase the content of organic or inorganic compounds e.g. of microbial
origin that causes the dust to be more reactive? (Differences between the two types of
dust)
4. Is the sensitivity of the subjects explaining the responses to exposures in a, b, or c?
(Subject group and sensitivity index)
As explorative investigations biomarkers for exposures and sensitivity for practical usage
are tested.
The study is focussed on two main questions:
c. The importance of dampness of the building and home dust as a factor of the subjects=
responses.
d. Can measures used in KLINIR predict the subjects’ responses to the dust?
As explorative investigations biomarkers for exposures and sensitivity are tested for
practical use.
These investigations are made during experimental exposures of subjects to dust from dry and
water damaged buildings. The responses of healthy KLINIR-sensitive subjects are predicted
using personal sensitivity measures.
The design is a 3x3 Latin square design (cross-over design). The subjects will be their own
controls and comparisons to placebo (clean air) were made. The study was double blinded and
the subjects were only informed about details on design and exposures after the experiment
and only if they asked.
This design eliminated effects of any learning or training during the investigations, and
also the effects of season and weekday was eliminated. The subjects were exposed with 3-4
weeks interval to eliminate carry-over of effects from one exposure session to the next.
The design was replicated three times on three different groups of subjects each including 9
subjects. Each group of nine were divided into three groups of three subjects.
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Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Prevention