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NCT03014661 Clinical Trial

Untersuchung Zur Erfassung Und Kontrolle Der Lebensqualität Unter Einer Therapie Mit Pollinex Quattro Bei Heuschnupfen

Rhinitis, Allergic, Seasonal Clinical Trial

Official title:
Untersuchung Zur Erfassung Und Kontrolle Der Lebensqualität Unter Einer Therapie Mit Pollinex Quattro Bei Heuschnupfen

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03014661
Other study ID # PQ-HOM-001
Secondary ID
Status Completed
Phase N/A
First received January 2, 2017
Last updated January 5, 2017
Start date June 2015
Est. completion date December 2015

Study information
Verified date January 2017
Source Saarland University
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Observational

Clinical Trial Summary

Questionnaire to measure and control the quality of life of patients with hay fever who are treated or were treated with Pollinex quattro

Description:

Questionnaire including 19 questions concerning the Quality of life of patients with hayfeyer under or after therapy with a specific immuntherapy with Pollinex quattro

Recruitment information / eligibility
Status Completed
Enrollment 58
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Pollinosis/seasonal Rhinitis based on an allergy against birch/alder/Hazel pollen OR grass/rye pollen OR mugwort

- Therapy with Polinex quattro

Exclusion Criteria:

- Age <18 years.

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Other:
• Quality of life under or after therapy with Pollinex quattro
To measure Quality of life using the DLQI-index in year one, year two, year three or six month after therapy with Pollinex quattro plus.

Locations
Country Name City State
Germany Saarland University Hospital. Department of Dermatology Homburg Saarland

Sponsors (1)
Lead Sponsor Collaborator
Saarland University

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Quality of life questionnaire (DLQI) during year one, year two, year three of therapy or within 6 months after completion of therapy No
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