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Inflammatory, Functional and Image Composite Measure to Define Asthma Control (APITA)

Primary Purpose

Asthma

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
prednisone
Sponsored by
Federal University of São Paulo
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring asthma, asthma control questionnaire, oral corticosteroid, air trapping, AQLQ, control, quality of life

Eligibility Criteria

16 Years - 80 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • A documented clinical asthma history at least for a period of six months
  • Regular treatment (IC + LABA) at least for a period of three months
  • Controlled symptoms score defined by GINA 2002 criteria (daytime symptoms < 2 days a week and no night time symptoms in the last 15 days) or complete absence of chronic symptoms
  • None or minimal exacerbations without emergency visits
  • Absent or a minimal usage bronchodilator rescue, side effects of medication and limitation to exercises
  • Documented airway reversibility of 200 ml and 7% based on predicted values of VEF1

Exclusion Criteria:

  • Having a smoking history of 5 pack/years or more; having other known chronic pulmonary diseases; having side effect to oral corticosteroid
  • Having an upper or lower respiratory tract infection within 4 weeks of visit 0
  • Unable to do the tests involved in the study.

Sites / Locations

  • Rua Botucatu 740 3 ° and - PneumologiaRecruiting

Outcomes

Primary Outcome Measures

Asthma control status characterized by nocturnal and diurnal symptom score FEV1,total lung capacity in plethysmography and reducing the air-tapping in HRCT.

Secondary Outcome Measures

Quality of life, Sputum and nasal cytology, adverse events

Full Information

First Posted
January 8, 2008
Last Updated
January 16, 2008
Sponsor
Federal University of São Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT00597064
Brief Title
Inflammatory, Functional and Image Composite Measure to Define Asthma Control
Acronym
APITA
Official Title
Inflammatory, Functional and Image Composite Measure to Define Asthma Control
Study Type
Interventional

2. Study Status

Record Verification Date
November 2007
Overall Recruitment Status
Unknown status
Study Start Date
July 2006 (undefined)
Primary Completion Date
March 2008 (Anticipated)
Study Completion Date
March 2008 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Federal University of São Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The goals of control status of asthma have been changed with the improvement of its management as a chronic disease; many steps should be taken to achieve asthma control as defined by the GINA/NIH guidelines. There are good results with single variables, but overall asthma control should be addressed in different ways. Most traditional clinical studies provide an incomplete assessment of disease control, despite good clinical practice. The association of inhaled corticosteroid (IC) and long-action beta 2 agonist (LABA) has already showed their efficacy to reduce asthma symptoms, exacerbations and cost for moderate and severe asthma patients as well as the improvement in their quality of life. On the other hand, even with the use of first line maintenance medication, as recommended by guidelines, some asthmatic patients fail in obtaining a total control of the disease. This lack of efficacy, led us to hypothesize, that these patients who fail in response, would present chronic and fixed airway obstruction as a consequence of persistent inflammation and airway remodeling. This study has the purpose of looking for an adequate composite measure to provide an indicator of overall asthma status more accurately and meaningfully as reflect of treatment effectiveness and disease control. For this, we will test by a randomized control trial if an additional oral corticosteroid treatment could modify spirometric and plethysmography values, nasal and low airway cytology and HRCT (to evaluate small airway) in regularly treated stable asthma patients who have a positive bronchodilator response.
Detailed Description
To evaluate the achievement of asthma control status in asthmatic patients, regularly treated with IC + LABA to answer the following questions: i. Is it possible to improve the pulmonary function (spirometry and plethysmography) of stable asthma patients, regularly treated with IC + LABA, who have a positive bronchodilator response, with the introduction of oral steroid? ii. What is the relationship among nasal, induced sputum and blood cytology, as a tool to observe inflammatory airway expression, in controlled and total controlled asthma patients? What will be these values response if oral steroids have been introduced? iii. What is the correlation between pulmonary volumes and airways inflammation to evaluate severity and control status in asthmatic patients, using plethysmography and HRCT? What will be these values response if oral steroids have been introduced?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
asthma, asthma control questionnaire, oral corticosteroid, air trapping, AQLQ, control, quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
prednisone
Other Intervention Name(s)
prednisone or placebo radom assigned
Intervention Description
oral prednisone 40 mg/day for 15 +/- 5 days
Primary Outcome Measure Information:
Title
Asthma control status characterized by nocturnal and diurnal symptom score FEV1,total lung capacity in plethysmography and reducing the air-tapping in HRCT.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Quality of life, Sputum and nasal cytology, adverse events
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: A documented clinical asthma history at least for a period of six months Regular treatment (IC + LABA) at least for a period of three months Controlled symptoms score defined by GINA 2002 criteria (daytime symptoms < 2 days a week and no night time symptoms in the last 15 days) or complete absence of chronic symptoms None or minimal exacerbations without emergency visits Absent or a minimal usage bronchodilator rescue, side effects of medication and limitation to exercises Documented airway reversibility of 200 ml and 7% based on predicted values of VEF1 Exclusion Criteria: Having a smoking history of 5 pack/years or more; having other known chronic pulmonary diseases; having side effect to oral corticosteroid Having an upper or lower respiratory tract infection within 4 weeks of visit 0 Unable to do the tests involved in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ana Luisa G Fernandes, MD, PhD
Phone
551150841268
Email
analgf@tewrra.com.br
First Name & Middle Initial & Last Name or Official Title & Degree
Maria Marta F Amorim, MSc
Phone
55 11 50841268
Email
martafamorim@terra.com.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ana Luisa G Fernandes, MD, PhD
Organizational Affiliation
Federal University of Sao Paulo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rua Botucatu 740 3 ° and - Pneumologia
City
São Paulo
State/Province
Sao Paulo
ZIP/Postal Code
04023062
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Marta F Amorim, MSc
Phone
55 11 50841268
Email
martafamorim@terra.com.br
First Name & Middle Initial & Last Name & Degree
Patricia B Lima, Techinician
Phone
55 11 50841268
Email
patricia@pneumo.epm.br
First Name & Middle Initial & Last Name & Degree
Ana Luisa G Fernandes, MD, PhD
First Name & Middle Initial & Last Name & Degree
Alexander Araruna, MD
First Name & Middle Initial & Last Name & Degree
Maria Marta F Amorim, MSc

12. IPD Sharing Statement

Links:
URL
http://www.unifesp.br/dmed/pneumo/posgraduacao.htm
Description
University home page

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Inflammatory, Functional and Image Composite Measure to Define Asthma Control

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