CClinicalTrials.gg
CompletedNCT00695357EPAGGELIAUpdated Apr 30, 2009

Opinion of Patients Under Treatment That Meets the Criteria of New Treatment Strategy According to GINA 2006

An observational study in New Strategies, GINA 2006 and Patient Opinion, sponsored by AstraZeneca. Completed at 31 sites in Greece. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2009-04-30.

Sponsored by AstraZeneca · Observational

Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
832
Ages
18 Years and older
Sex
All
01

Study summary

Cross-sectional, one visit study. All the data will be collected through questionnaires. Descriptives statistics will be applied to the data. 832 patients will participate to the study and 104 physicians.

02

Conditions studied

  • New Strategies
  • GINA 2006
  • Patient Opinion

Keywords

  • Asthma treatment
  • GINA 2006
  • patient perception
03

In context

Lead sponsor

AstraZeneca is the lead sponsor of 3,429 studies on the registry; 270 are open to participants now.

Of its 357 completed or terminated interventional studies of FDA-regulated products, 173 (48%) have results posted.

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

04

Who can participate

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

Study population

Primary care

Inclusion criteria

  • Patients diagnosed with persistent asthma (GINA 2005) for at least 6 months before entering the study
  • Patients who are under treatment according to the new strategies described in GINA 2006 for at least 3 months before entering the study

Exclusion criteria

Exclusion Criteria:

  • Patients who are not willing to sign the Informed Consent Form
  • COPD Patients
05

Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
832 participants (estimated)
06

What researchers measure

Primary outcomes

  1. Percentage (%) of Asthma treatment satisfaction and control grading

    Time frame: single visit / once

Secondary outcomes

  1. Rate of treatment compliance

    Time frame: single visit / once

  2. Patients quality of life under treatment

    Time frame: single visit / once

07

Study locations

31 sites
  • Research Site
    Aleksandroupoli, Greece
  • Research Site
    Amaliada, Greece
  • Research Site
    Argos, Greece
  • Research Site
    Arta, Greece
  • Research Site
    Athina, Greece
  • Research Site
    Chania, Greece
  • Research Site
    Drama, Greece
  • Research Site
    Githio, Greece
  • Research Site
    Gounari, Greece
  • Research Site
    Imathia, Greece
  • Research Site
    Ioannina, Greece
  • Research Site
    Iraklio, Greece
  • Research Site
    Kalamata, Greece
  • Research Site
    Katerini, Greece
  • Research Site
    Kavala, Greece
  • Research Site
    Komotini, Greece
  • Research Site
    Lamia, Greece
  • Research Site
    Larisa, Greece
  • Research Site
    Nafpaktos, Greece
  • Research Site
    Neapoli, Greece
  • Research Site
    Patra, Greece
  • Research Site
    Pirgos, Greece
  • Research Site
    Rafina, Greece
  • Research Site
    Serres, Greece
  • Research Site
    Sparti, Greece
  • Research Site
    Thessaloniki, Greece
  • Research Site
    Trikala, Greece
  • Research Site
    Tripoli, Greece
  • Research Site
    Veria, Greece
  • Research Site
    Volos, Greece
  • Research Site
    Xalkida, Greece
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 30, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00695357
Lead sponsor
AstraZeneca
First posted
Jun 11, 2008
Start date
Apr 2008
Completion
Jun 2008
Last update
Apr 30, 2009

Study contacts

Zachariadis Manolis, MD
principal investigator · Euroclinic, Athens, Greece

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2009. You cannot join it, but the record below documents what was studied.

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