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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01475045
Other study ID # 20109-HAL-EL-02
Secondary ID Sponsor ID
Status Completed
Phase N/A
First received October 12, 2011
Last updated November 18, 2011
Start date January 2011
Est. completion date September 2011

Study information

Verified date November 2011
Source Elpen Pharmaceutical Co. Inc.
Contact n/a
Is FDA regulated No
Health authority Greece: National Organization of Medicines
Study type Observational

Clinical Trial Summary

The aim of the study is to compare patients' satisfaction from the use of three different inhalation devices by using the FSI-10 questionnaire


Description:

Patients are requested to reply to FSI-10 questionnaire regarding their satisfaction from inhalation devices. Patients are on 3 different asthma inhalation devices with combination treatment (Turbuhaler, Diskus, Elpenhaler)


Recruitment information / eligibility

Status Completed
Enrollment 1160
Est. completion date September 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients > 18 years old, both genders who are on their inhalation treatment at least two months before study enrollment,

- Who are able to be compliant to study procedures

Exclusion Criteria:

- Patients < 18 years old,

- Patients who are on their inhalation treatment less than two months before study enrollment

- Patients who are not able to be compliant to study procedures

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Greece 7th Pulmonary Clinic, Sotiria Hospital Athens
Greece Sotiria Hospital Athens

Sponsors (1)

Lead Sponsor Collaborator
Elpen Pharmaceutical Co. Inc.

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patients' satisfaction Patients' replies to FSI-10 questionnaire valid in Greek language all study period (5 months) No
Secondary Patients devices' use all study period (5 months) No
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