Asthma Clinical Trial
— SCITOfficial title:
The Effect of Pollen Season on Subcutaneous Allergen Immunotherapy Reactions: A Double Blind Randomized Control Trial.
Subcutaneous allergen immunotherapy (SCIT) is a widely used and effective treatment modality
for allergic rhinoconjunctivitis and asthma. SCIT starts with a build-up phase during which a
patient receives frequent, escalating doses of the allergens they are allergic to until they
reach a predetermined maintenance dose. This is followed by a maintenance phase during which
the allergen dose is kept constant and administered at greater intervals. Maximum clinical
improvement is generally not seen until a patient is in the maintenance phase. Anecdotal
evidence of possible reactions to SCIT administered during a patient's pollen season has led
to dosage freezes during a patient's pollen season which extends the length of the build-up
phase by many months. Prolonging the buildup phase increases the time required to obtain
maximal benefit from SCIT, and at the same time, can decrease patient compliance with therapy
due to the prolonged period of time when frequent injections are required.
The aims of this study are to determine if adverse reactions to pollen SCIT are increased if
doses are increased during pollen season.
Status | Unknown status |
Enrollment | 245 |
Est. completion date | April 2014 |
Est. primary completion date | April 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 5 Years and older |
Eligibility |
Inclusion Criteria: - include individuals ages 5 and greater at Allergy/Immunology Associates, Inc., who are receiving build-up SCIT to tree, grass, and/or weed pollens for allergic rhinitis, allergic conjunctivitis, and/or asthma Exclusion Criteria: 1. are in maintenance phase of SCIT 2. are on beta-blockers 3. have a forced expiratory volume in 1 second (FEV1) of less than 70% of predicted 4. have a history of anaphylaxis with previous SCIT to aeroallergens (as defined by the requirement of intramuscular or subcutaneous epinephrine for treatment of a SCIT-induced reaction) 5. have any uncontrolled cardiac or pulmonary disease as determined by their treating allergist/immunologist 6. are pregnant, due to risk of harm to fetus if anaphylaxis occurs. |
Country | Name | City | State |
---|---|---|---|
United States | Allergy/Immunology Associates Inc. | South Euclid | Ohio |
Lead Sponsor | Collaborator |
---|---|
University Hospitals Cleveland Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Immediate Reaction Rate of Build-Up Phase in Pollen Season | To determine if escalating pollen SCIT doses during the pollen season is associated with an increased rate of immediate reactions in comparison to holding SCIT doses constant. | 1 year | |
Secondary | Delayed Reaction Rate of Build-Up Phase during Pollen Season | To determine if escalating pollen SCIT doses during the pollen season is associated with an increased rate of delayed reactions in comparison to holding SCIT doses constant. | 1 year. |
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