Corn Occupational Rhinitis SCIT Efficacy Study
NCT02949050 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2018-05-02
Summary
Patients demonstrated allergic to corn pollen and timothy grass pollen (by allergy testing) who have undergone 1 to 2 years of subcutaneous allergen immunotherapy (SCIT) containing timothy grass extract with moderate symptomology (as documented via rhinitis symptom score surveys) will constitute the treatment group. Those who previously chose not to undergo SCIT who have documented symptomology and are skin test positive to corn pollen will constitute the control group. Prospective symptom score analyses and retrospective quality of life assessments (RQLQ) will be the primary and secondary efficacy outcome measures.
Conditions
- Rhinitis
Interventions
- BIOLOGICAL
-
subcutaneous allergen immunotherapy (SCIT)
20 patients who (prior to study enrollment and initiation) completed more than 1 year of timothy grass SCIT vs. 20 control patients who underwent corn pollen exposure for for greater than one year during the same prestudy time interval. Efficacy will be assessed by analyses of symptom score surveys and quality of life surveys.
- BIOLOGICAL
-
SCIT
Treatment group consists of patients who completed \> 1 year of SCIT while control group patients did not undergo SCIT
Sponsors & Collaborators
-
United Allergy Services
lead INDUSTRY
Principal Investigators
-
frederick m schaffer, md · United Allergy Services
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 10 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2016-08-31
- Primary Completion
- 2016-11-30
- Completion
- 2018-12-31
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