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Molekule for Allergic Rhinitis/Asthma

Molekule for Allergic Rhinitis/Asthma

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03627689
Enrollment
49
Registered
2018-08-13
Start date
2018-07-13
Completion date
2019-01-31
Last updated
2019-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic Conjunctivitis, Allergic Rhinitis, Asthma

Keywords

asthma, environmental intervention, allergies, air purifier

Brief summary

Exposure to airborne allergens and pollutants is linked to symptom severity of allergies, asthma and other respiratory problems. In this study an air purifier using photo-electrochemical oxidation technology (PECO) will be used in the home environment of study participants. The investigator will assess the reduction of symptoms from allergic rhinitis/conjunctivitis and asthma.

Detailed description

The purpose of this study is to assess the efficacy of the portable PECO air purifier in reducing symptoms from allergic rhinitis and asthma. Using a randomized, double blinded placebo, controlled trial we will be then able to assess if there are any changes after the use of the PECO air purifier after completing an initial baseline survey & comparing to the exit survey. This is a double-blind study, which means that neither the participant nor the investigator knows which device is being used until after the trial is over.

Interventions

OTHERActive air purifier in respiratory allergies/asthma

Continuous use of air purifier to improve allergies and asthma control

control arm

Sponsors

Molekule
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Chronic allergic rhinitis and/or conjunctivitis by history 2. History of adult asthma requiring medications now or in the past 3. Age ≥18 4. CARAT score less than 24

Exclusion criteria

1. Participant is \<18 years-old 2. Use of systemic corticosteroids within 14 days of study initiation 3. Treatment with biologic agents or allergen immunotherapy 4. Treatment with other immunomodulators (cyclosporine, azathioprine, hydroxychloroquine, etc) 5. Sensitive to fan sound or blue/purple light at night time

Design outcomes

Primary

MeasureTime frameDescription
Control of Allergic Rhinitis and Asthma Test (CARAT) score4 weeksCARAT will measure the change in control scores of respiratory allergies and asthma. Scale 0 (Worse control of allergy and asthma) to 30 (Best control of allergy and asthma). The higher score the better control of allergy and asthma. There are 10 individual questions, scoring from 0-3.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026