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Evaluation of a New Self-assessed, Home-based Symptom Score in Cat Allergic Patients

Evaluation of a New Self-assessed, Home-based Symptom Score in Cat Allergic Patients

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02959073
Acronym
HypoScore-2
Enrollment
10
Registered
2016-11-08
Start date
2016-09-30
Completion date
2017-02-28
Last updated
2017-05-03

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

Conditions

Cat Allergy

Keywords

Symptom recording

Brief summary

In the last decades the prevalence of allergies has reached epidemic proportions. 10 to 15% of the population suffers from cat allergy. Investigators perform this study in order to further investigate symptom records and their evaluation in cat allergic patients. Investigators primarily aim to better standardize the symptom recording of cat allergic persons under real-life conditions and to evaluate the effect of hypoallergenic cats on symptom strength.

Interventions

OTHERSymptom Recording

Subjects muss record their allergic symptoms after contact with their cats

Sponsors

Ottawa Allery Research Corporation
CollaboratorUNKNOWN
University of Zurich
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Participant understands the nature, meaning and scope of the study. * Signed Informed Consent after being informed. * Male and Female patients 18 years to 65 years of age. * Positive screening prick test (mean wheal diameter equal or greater 3 mm) when tested with already standardized cat allergen extract. * Positive screening prick test (wheal diameter equal or greater 3mm) to Histamine dihydrochloride 10 mg/ml. * Positive Scratch Test when tested with cat dander sample of participant's cat. * Baseline symptoms with a severity of 1 in at least 2 different symptoms. * Owner of a cat that lives in the same household. * Cat will not have been washed in the 4 weeks before starting the test phase.

Exclusion criteria

* Impaired in understanding the nature, meaning and scope of the study or incapable of giving written informed consent * Participation in another study with investigational drug within the 30 days preceding and during the present study * Women who are pregnant or breast feeding * Intention to become pregnant during the course of the study * Positive skin reaction in the prick test to negative control * History of anaphylactic reaction to pet allergens * Severe diseases influencing the results of the present study by discretion of the investigator * Immunotherapy with fel d 1 / cat allergen preparation during the past two years * Skin lesions and excessive hair-growth in the skin test areas * Treatment with prohibited concomitant medications according to section 8.3 with the exception of medications with local effects which will not influence the results of the skin tests and the results of the other tests (testing period). * The patient should not suffer from other respiratory allergies during this study

Design outcomes

Primary

MeasureTime frameDescription
Duration of provocation test under 2 different conditionsup to 9 weeks
Number of score Points resulting from symptom recordup to 9 weeks
fel d 1 concentration in cat danderup to 9 weeksby collecting cat's fur
fel d 1 concentration in the airup to 9 weeksby means of electrostatic dust collectors papers

Countries

Canada

Outcome results

None listed

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