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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01251224
Other study ID # 1U01AI083238
Secondary ID
Status Completed
Phase Phase 3
First received November 29, 2010
Last updated March 15, 2017
Start date November 2010
Est. completion date September 2016

Study information

Verified date March 2017
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The MAAIT is a randomized, controlled trial of a home intervention to reduce mouse allergen exposure in mouse allergic children with asthma and mouse allergen exposure. Participants will be randomized to either the Integrated Pest Management (IPM) Group or the Education Group. The IPM Group will receive professional mouse abatement, education, two HEPA filters, allergen-proof mattress and pillow encasements, and targeted cleaning. The Education Group will receive education about IPM at the beginning of the trial and then after completion of the trial, will receive the IPM intervention. Participants will be followed for 12 months.


Recruitment information / eligibility

Status Completed
Enrollment 361
Est. completion date September 2016
Est. primary completion date September 2016
Accepts healthy volunteers No
Gender All
Age group 6 Years to 17 Years
Eligibility Inclusion Criteria:

- persistent asthma

- exacerbation, previous 12 months

- evidence of mouse sensitization

- high levels of mouse allergen in home

- ages 5-17 years

Exclusion Criteria:

- intermittent asthma

- no exacerbation in previous 12 months

- not sensitized to mouse

- low or undetectable mouse allergen in home

- other lung disease aside from asthma

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Integrated Pest Management
The IPM intervention will include professional mouse abatement, two HEPA filters, targeted cleaning, education about IPM, and allergen-proof mattress and pillow encasements. The intervention will be delivered at baseline to the IPM Group, and then repeated if recurrent or persistent mouse infestation is present.
Education
This group will receive education about mouse IPM.

Locations

Country Name City State
United States Johns Hopkins Baltimore Maryland
United States Boston Children's Boston Massachusetts

Sponsors (3)

Lead Sponsor Collaborator
Johns Hopkins University Boston Children’s Hospital, Columbia University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in asthma symptoms days of asthma symptoms 0, 3, 6, 9, 12 months
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