COMPLliancE and qualiTy of lifE in Asthma

Asthma Clinical Trial

— COMPLETE  

Official title:

Multicenter, Open-label, Non Interventional, Prospective, Observational Clinical Trial to Assess the Compliance and Quality of Life in Greek Asthmatic Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03300076
• Other study ID #: 2017-HAL-EL-74
• Status: Completed
• Start date: February 1, 2018
• Est. completion date: December 1, 2018

Study information

• Verified date: March 2018
• Source: Elpen Pharmaceutical Co. Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

A multicenter, open, non-interventional, prospective, clinical observational study on Conformity to Therapy and Quality of Life in Asthma in patients living in Greece

Description:

Dry powder devices, available since 1970, have been developed to make inhalation simpler than pMDIs and relieve the need for co-ordination of spraying and inhalation, which is particularly important for patient groups such as the elderly and children. In addition, dry powder devices do not contain propellant gases potentially hostile to the environment as they are activated by inhalation of the patient and do not cause cold sensation upon inhalation.

Today, the combination of inhaled corticosteroid (ICS) and long-acting β2-inducer with an inhaler is the basic treatment for asthma6.

The addition of long-acting β2-inducer (LABA) to a daily inhaled corticosteroid regimen1:

• Improves the symptoms,

• Reduces nightly asthma symptoms,

• Improves pulmonary function,

• Reduces the use of β2-agonists for rapid action,

• Reduces the number of seizures,

• Does not increase the risk of hospitalizations due to asthma,

• Achieves clinical asthma control in more patients, faster and with less ICS than would be required if ICS were administered alone.

The greater effectiveness of combination therapy has led to the development of stable combination inhalers that both glucocorticosteroids and LABA (eg, fluticasone-salmeterol, budesonide-formoterol stable compounds) are concomitantly conveyed.

Stable combinations are more user-friendly for patients, potentially increasing compliance, and ensure that LABA is always accompanied by glucocorticosteroid1. Of the combinations available, the budesonide-formoterol combination can be used both as maintenance therapy and symptom relief due to the rapid onset of formoterol compared to salmeterol. Both components of the budesonide-formoterol combination when administered are helpful in enhancing protection from severe seizures in patients receiving combination therapy for maintenance and improve the control of asthma at relatively low ICS doses.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 800
• Est. completion date: December 1, 2018
• Est. primary completion date: December 1, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Male or female asthma patients over 18 years of age

• Compliance with treatment

• Compliance with study procedures

• Signed informed consent form

• Patients not satisfactorily controlled with inhaled corticosteroids and the use of inhaled short-acting ß2-primers or patients already adequately controlled with both inhaled corticosteroids and long-acting ß2-stimulants:

1. Patients receiving ICS inhaled and SABA invoked

2. Patients receiving inhaled ICS and LABA with separate devices each

3. Patients receiving periodic and not continuously stable combination of ICS and LABA but not being treated for at least 1 month

4. Patients who did not receive any treatment and the doctor decides to immediately start the fixed combination of ICS and LABA

Exclusion Criteria:

• Male or female asthma patients under 18 years of age

• Unsigned patient consent

• Non-compliance with treatment

• Non-compliance in study procedures

• COPD patients (at any stage)

Related Conditions & MeSH terms

• Asthma
• Compliance, Patient
• Quality of Life

Locations

Country	Name	City	State
Greece	Sotiria Pulmonary 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	Quality of Life	Change in mini AQLQ scale	6 months
Secondary	Compliance	Change in MMAS-8 scale	6 months