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NCT Number: NCT00728715

Efficacy of Budesonide-Formoterol in Bronchiectasis

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital General de Requena

Valencia, 43260, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

budesonide-formoterol single inhaler

Drug

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

Other names: B. High-dose budesonide arm, A. Medium dose of budesonide plus formoterol

High dose of budesonide

Drug

1600 mcg/d of budesonide

A

Drug

medium dose of budesonide-formoterol

B

Drug

High Dose Inhaled Budesonide

Primary outcomes

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

    Time frame: at 3 and 6 months

Secondary outcomes

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

    Time frame: at 3 and 6 months

Sponsors and collaborators

Lead sponsor

Hospital General de Requena

Other

Collaborators

  • Esteve

Registry information

Official study title

Clinical Efficacy and Safety of Budesonide and Formoterol in the Management of Non-Cystic Fibrosis Bronchiectasis

Important dates

Study start
2004
Primary completion
2005
Study completion
2005
First posted
Aug 6, 2008
Registry last updated
Aug 6, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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