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OpenTrials
Completed

NCT Number: NCT03014661

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

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Saarland University Hospital. Department of Dermatology

Homburg, Saarland, 66421, Germany

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Quality of life under or after therapy with Pollinex quattro

Other

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.

Primary outcomes

  1. Quality of life questionnaire (DLQI)

    Time frame: during year one, year two, year three of therapy or within 6 months after completion of therapy

Sponsors and collaborators

Lead sponsor

Universität des Saarlandes

Other

Registry information

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Jan 9, 2017
Registry last updated
Jan 9, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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