CClinicalTrials.gg
TerminatedNCT02041624ALTOUpdated Apr 18, 2016

International Registry on the Quality of Life of Patients With Grass-pollen-induced Allergic Rhinitis

An observational study in Allergic Rhinitis Due to Grass Pollens, sponsored by Stallergenes Greer. Terminated at 1 site in France. Open to participants aged 5 Years and older. Per ClinicalTrials.gov, last updated 2016-04-18.

Sponsored by Stallergenes Greer · Observational

Why this study was terminated
Sponsor decision
Study type
Observational
Time perspective
Prospective
Enrollment
740
Ages
5 Years and older
Sex
All
01

Study summary

The purpose of the present study is to describe patient's perception of quality of life and effectiveness of ORALAIR® over a follow-up period up to 5 years, in real-life settings.

Read the detailed description

Primary objective:

To describe the patient's perception of the impact of ORALAIR® on his/her health related generic and disease specific quality of life during the grass pollen season in real-life settings.

Secondary objectives:

  • To describe the patient's perceived effectiveness of ORALAIR® in allergic rhinoconjunctivitis management in terms of disease intensity, satisfaction and rescue medication
02

Conditions studied

  • Allergic Rhinitis Due to Grass Pollens

Keywords

  • allergic
  • rhinitis
  • conjunctivitis
  • grass pollen
  • Allergen ImmunoTherapy (AIT)
  • grass mix
03

In context

Rhinitis

1,105 studies on the registry are indexed under Rhinitis; 65 are open to participants now.

This study's enrollment of 740 is above the median of 141 across 172 observational studies indexed under Rhinitis.

Browse Rhinitis studies →

Lead sponsor

Stallergenes Greer is the lead sponsor of 25 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients with allergic rhino-conjunctivitis are visiting their allergist during grass-pollen season when symptoms are strong. In accordance with the terms of the Marketing Authorization, ORALAIR® treatment has to be set-up "at the right moment" about 4 months before the next grass-pollen season.

Inclusion criteria

  • Patient of 5 years of age and older at the date of the screening visit
  • Patient with proven allergic rhino-conjunctivitis due to grass pollen
  • Patient eligible for a grass-pollen Allergen ImmunoTherapy (AIT)
  • Patient whose physician prescribed ORALAIR® independently of the study, before the beginning of the grass-pollen season

Exclusion criteria

Exclusion Criteria:

  • Patient participating in a clinical trial or in an epidemiological study
05

Study design

Time perspective
Prospective
Enrollment
740 participants (actual)
Target follow-up
5 Years
Patient registry
Yes

Groups and cohorts

  • allergic rhino-conjunctivitis

    Patient with proven allergic rhino-conjunctivitis due to grass pollen

06

What researchers measure

Primary outcomes

  1. Health related quality of life

    The primary objective is to describe the patient's perception of the impact of ORALAIR® on his/her health related generic and disease specific quality of life during the grass-pollen season in real-life settings.

    Time frame: patients will be followed for the duration of the treatment, an expected average of 6 months/year

Secondary outcomes

  1. Treatment Effectiveness

    To describe the patient's perceived effectiveness of ORALAIR® in allergic rhino-conjunctivitis management in terms of disease intensity, satisfaction and rescue medication

    Time frame: patients will be followed for the duration of the treatment, an expected average of 6 months/year

07

Study locations

1 site
  • Laboratoire Stallergenes
    Antony, 92183, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 18, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02041624
Lead sponsor
Stallergenes Greer
Collaborators
Registrat-Mapi
Responsible party
Sponsor
First posted
Jan 22, 2014
Start date
May 2014
Primary completion
Dec 2015
Completion
Dec 2015
Last update
Apr 18, 2016

Study contacts

Alain DIDIER, MD
principal investigator · Hôpital Larrey, Toulouse, France

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Apr 2016. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion