- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00695357
Opinion of Patients Under Treatment That Meets the Criteria of New Treatment Strategy According to GINA 2006 (EPAGGELIA)
April 29, 2009 updated by: AstraZeneca
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.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Anticipated)
832
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
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
- Research Site
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Primary care
Description
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:
- Patients who are not willing to sign the Informed Consent Form
- COPD Patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Percentage (%) of Asthma treatment satisfaction and control grading
Time Frame: single visit / once
|
single visit / once
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Rate of treatment compliance
Time Frame: single visit / once
|
single visit / once
|
Patients quality of life under treatment
Time Frame: single visit / once
|
single visit / once
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Zachariadis Manolis, MD, Euroclinic, Athens, Greece
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2008
Study Completion (Actual)
June 1, 2008
Study Registration Dates
First Submitted
June 9, 2008
First Submitted That Met QC Criteria
June 9, 2008
First Posted (Estimate)
June 11, 2008
Study Record Updates
Last Update Posted (Estimate)
April 30, 2009
Last Update Submitted That Met QC Criteria
April 29, 2009
Last Verified
April 1, 2009
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- NIS-RGR-DUM-2008/1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on New Strategies
-
AstraZenecaCompleted
-
Valduce HospitalCompletedResect and Discard Strategies for ColonoscopyItaly
-
Uppsala UniversityCompletedImplementation Strategies | Nutritional Outcome of Nursing Home ResidentsSweden
-
Bispebjerg HospitalCompletedRehabilitation Strategies for Elderly Post-Operative PatientsDenmark
-
Cardiovascular Center FrankfurtSheba Medical Center; Kerstin Piayda, CardioVascular Center Frankfurt, Frankfurt... and other collaboratorsActive, not recruitingRisk Factors | Left Atrial Appendage Occluder | Device Embolisation | Therapy StrategiesGermany
-
Davinia WithingtonUnknownSedation | Mechanical Ventilation | Daily Sedative Interruption | Sedation Strategies | Sedation ProtocolsCanada
-
Gerencia De Atencion Primaria Area 2 De MadridHealth Research Fund of ISCIII SpainCompletedCardiovascular Risk Factors | Primary Care | Clinical Practice Guideline | Implementation StrategiesSpain
-
University of HohenheimGerman Federal Ministry of Education and ResearchCompletedPharmacokinetics of New Curcumin Formulations | Safety of New Curcumin FormulationsGermany
-
University of Texas at AustinRecruitingPediatric Cancer | Grief | Bereavement | Well-Being, Psychological | Coping StrategiesUnited States
-
Duke UniversityTerminatedPain Management Strategies in Liver Resection SurgeryUnited States