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Efficacy of Budesonide-Formoterol in Bronchiectasis

Primary Purpose

Bronchiectasis

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
budesonide-formoterol single inhaler
High dose of budesonide
A
B
Sponsored by
Hospital General de Requena
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bronchiectasis focused on measuring Budesonide, Formoterol, Non cystic fibrosis bronchiectasis

Eligibility Criteria

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

Inclusion Criteria:

  • 18-80 years old patients diagnosed of non-cystic fibrosis bronchiectasis
  • More than 1 pulmonary lobe affected
  • Chronic obstructive airflow obstruction
  • Stable phase of the disease

Exclusion Criteria:

  • Asthma, COPD or current/past smnokers
  • No consent
  • Known intolerance to budesonide or formoterol

Sites / Locations

  • Hospital General de Requena

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

A

B

Arm Description

Medium Dose of budesonide-formoterol

High dose of inhaled budesonide (1600 mcg/day)

Outcomes

Primary Outcome Measures

Health related quality of life (measured by St Gorge Respiratory Questionnaire)

Secondary Outcome Measures

Forced spirometry; microbiological data, clinical data (dyspnea, cough, wheezes) and side effects

Full Information

First Posted
July 31, 2008
Last Updated
July 31, 2008
Sponsor
Hospital General de Requena
Collaborators
Esteve
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1. Study Identification

Unique Protocol Identification Number
NCT00728715
Brief Title
Efficacy of Budesonide-Formoterol in Bronchiectasis
Official Title
Clinical Efficacy and Safety of Budesonide and Formoterol in the Management of Non-Cystic Fibrosis Bronchiectasis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2008
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
January 2005 (Actual)
Study Completion Date
January 2005 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Hospital General de Requena
Collaborators
Esteve

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Some studies have concluded that high-dose inhaled steroids (IS) are effective in the clinical control of patients with bronchiectasis, however the high doses needed provokes some adverse effects and lower doses are not effective. Combined treatment with budesonide and formoterol have demostrated to be effective in patients with asthma and COPD achieving the reduction of steroid dose thanks to the adition of a long-acting beta 2 agonists. There are no studies in the literature analysing the effect of combined treatment in patients with bronchiectasis. The objective of this study is to compare the efficacy and safety of formoterol-medium dose of budesonide in a single inhaler versus high-dose of budesonide in the clinical control of patientes with non-cystic fibrosis bronchiectasis. Study Design: Randomized (3 months) parallel groups study. Patients: Patients with bronchiectasis diagnosed by high-resolution CT scan and chronic obstructive airway obstruction. Exclusion: Asthma and current or past smokers. Methods: Run in period in all patients with high dose of budesonide (1600 mcg/day) for 3 months. After that, randomization into two groups: 1. The same treatment (1600 mcg/day of budesonide) or combined treatment with lower dose of budesonide (18 mcg/day of formoterol and 800 mcg of budesonide) in a single turbuhaler inhaler during 3 months. Studied variables: Clinical, functional, quality of life, microbiological and number of side effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchiectasis
Keywords
Budesonide, Formoterol, Non cystic fibrosis bronchiectasis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Medium Dose of budesonide-formoterol
Arm Title
B
Arm Type
Active Comparator
Arm Description
High dose of inhaled budesonide (1600 mcg/day)
Intervention Type
Drug
Intervention Name(s)
budesonide-formoterol single inhaler
Other Intervention Name(s)
B. High-dose budesonide arm, A. Medium dose of budesonide plus formoterol
Intervention Description
High dose budesonide:Budesonide (Pulmocort turbuhaler) 400 mcg (2 inhalations bid) Medium dose budesonide plus formoterol (Rilast turbuhaler) 4,5 mcg of formoterol plus 400 mcg of budesonide: 2 inhalations bid
Intervention Type
Drug
Intervention Name(s)
High dose of budesonide
Intervention Description
1600 mcg/d of budesonide
Intervention Type
Drug
Intervention Name(s)
A
Intervention Description
medium dose of budesonide-formoterol
Intervention Type
Drug
Intervention Name(s)
B
Intervention Description
High Dose Inhaled Budesonide
Primary Outcome Measure Information:
Title
Health related quality of life (measured by St Gorge Respiratory Questionnaire)
Time Frame
at 3 and 6 months
Secondary Outcome Measure Information:
Title
Forced spirometry; microbiological data, clinical data (dyspnea, cough, wheezes) and side effects
Time Frame
at 3 and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18-80 years old patients diagnosed of non-cystic fibrosis bronchiectasis More than 1 pulmonary lobe affected Chronic obstructive airflow obstruction Stable phase of the disease Exclusion Criteria: Asthma, COPD or current/past smnokers No consent Known intolerance to budesonide or formoterol
Facility Information:
Facility Name
Hospital General de Requena
City
Valencia
ZIP/Postal Code
43260
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
21778259
Citation
Martinez-Garcia MA, Soler-Cataluna JJ, Catalan-Serra P, Roman-Sanchez P, Tordera MP. Clinical efficacy and safety of budesonide-formoterol in non-cystic fibrosis bronchiectasis. Chest. 2012 Feb;141(2):461-468. doi: 10.1378/chest.11-0180. Epub 2011 Jul 21.
Results Reference
derived

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Efficacy of Budesonide-Formoterol in Bronchiectasis

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