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Immunotherapy Administered Under the Tongue to Treat Dust Mite Allergy

Primary Purpose

Asthma

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
House Dust Mite SLIT
High dose SLIT
Placebo SLIT
Sponsored by
University of Wisconsin, Madison
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring Breathing, Allergy, Mites, House Dust

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: House dust mite-induced allergic rhinitis/mild intermittent asthma Exclusion Criteria: Use of previous allergy immunotherapy for house dust mite asthma Pregnancy or breastfeeding

Sites / Locations

  • University of Wisconsin Medical School

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Low dose SLIT

High dose SLIT

Placebo

Arm Description

Low dose SLIT

High dose SLIT

Placebo

Outcomes

Primary Outcome Measures

Bronchial Threshold to Allergen Challenge From Baseline to 12-18 Months of Treatment
Antigen challenge was performed using the antigen house dust mite. Increasing doses of antigen were inhaled and then lung function (using the procedure Spirometry, measuring Forced Expiatory Volume in the 1st second FEV1) was measured after each dose. The challenge was stopped once the lung function (FEV1) was dropped by 20% of percent predicted. The dose of antigen that caused a 20% drop in lung function is considered the bronchial threshold. The higher the dose of antigen that causes the drop in lung function, the higher tolerance a participant has of inhaling house dust mite. This dose was measure at baseline and then again after 12-18 months of treatment with sublingual house dust mite antigen.Cumulative breath units is the unit of measure to indicate how much antigen is tolerated before the FEV1 is dropped by 20%. Cumulative breath units is also known as breath units.

Secondary Outcome Measures

Full Information

First Posted
September 13, 2005
Last Updated
May 21, 2019
Sponsor
University of Wisconsin, Madison
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00200850
Brief Title
Immunotherapy Administered Under the Tongue to Treat Dust Mite Allergy
Official Title
Sublingual Immunotherapy in Dust Mite Allergy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
January 2006 (Actual)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
October 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Wisconsin, Madison
Collaborators
National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will investigate sublingual immunotherapy (SLIT), a treatment involving antigens placement under the tongue to help asthma sufferers build a tolerance to the allergy-causing substances. Specifically, this study will determine the effectiveness of SLIT at two different dosing regimens for patients with intermittent mild asthma caused by dust mites.
Detailed Description
Asthma is a serious lung condition that is the leading cause of long-term illness in children. Many common household substances can trigger or worsen an asthma attack. It is important for people to reduce household allergens and learn effective treatments for specific types of asthma. Inhaled short-acting beta agonist such as albuterol is the standard treatment for mild, intermittent asthma. However, recent studies have shown that adding allergen-specific immunotherapy to your current asthma therapy can help to control asthma symptoms. This study will determine the safety and effectiveness of SLIT in two different dosing regimens in treating patients with house dust mite-induced allergic rhinitis/mild intermittent asthma. Participants will be randomly assigned to receive low dose SLIT, high dose SLIT, or placebo for at least 12 months. House dsut mite-induced allergy skin tests will be performed at study entry, at selected timepoints throughout the study, and at the end of the study. The tests will determine whether SLIT creates an immune tolerance state as well as whether SLIT acts via local or systemic immunological systems.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Breathing, Allergy, Mites, House Dust

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Low dose SLIT
Arm Type
Active Comparator
Arm Description
Low dose SLIT
Arm Title
High dose SLIT
Arm Type
Active Comparator
Arm Description
High dose SLIT
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Biological
Intervention Name(s)
House Dust Mite SLIT
Intervention Description
low dose SLIT 143 Allergen Units(AU)/ml daily
Intervention Type
Biological
Intervention Name(s)
High dose SLIT
Intervention Description
House Dust Mite SLIT- 10,000 Allergen units(AU)/ml daily
Intervention Type
Biological
Intervention Name(s)
Placebo SLIT
Intervention Description
Placebo SLIT daily
Primary Outcome Measure Information:
Title
Bronchial Threshold to Allergen Challenge From Baseline to 12-18 Months of Treatment
Description
Antigen challenge was performed using the antigen house dust mite. Increasing doses of antigen were inhaled and then lung function (using the procedure Spirometry, measuring Forced Expiatory Volume in the 1st second FEV1) was measured after each dose. The challenge was stopped once the lung function (FEV1) was dropped by 20% of percent predicted. The dose of antigen that caused a 20% drop in lung function is considered the bronchial threshold. The higher the dose of antigen that causes the drop in lung function, the higher tolerance a participant has of inhaling house dust mite. This dose was measure at baseline and then again after 12-18 months of treatment with sublingual house dust mite antigen.Cumulative breath units is the unit of measure to indicate how much antigen is tolerated before the FEV1 is dropped by 20%. Cumulative breath units is also known as breath units.
Time Frame
baseline and after 12-18 months treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: House dust mite-induced allergic rhinitis/mild intermittent asthma Exclusion Criteria: Use of previous allergy immunotherapy for house dust mite asthma Pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert K. Bush, MD
Organizational Affiliation
University of Wisconsin Medical School
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Wisconsin Medical School
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53706
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21333346
Citation
Bush RK, Swenson C, Fahlberg B, Evans MD, Esch R, Morris M, Busse WW. House dust mite sublingual immunotherapy: results of a US trial. J Allergy Clin Immunol. 2011 Apr;127(4):974-81.e1-7. doi: 10.1016/j.jaci.2010.11.045. Epub 2011 Feb 18. Erratum In: J Allergy Clin Immunol. 2011 Jun;127(6):1561. Morris, Mary [added].
Results Reference
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Immunotherapy Administered Under the Tongue to Treat Dust Mite Allergy

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