Status:

COMPLETED

A Proof of Concept Study to Evaluate the Dose Response for the Systemic Benefit Risk Ratio of Inhaled Fluticasone Propionate in Chronic Obstructive Pulmonary Disease

Lead Sponsor:

University of Dundee

Conditions:

COPD

Eligibility:

All Genders

50-90 years

Phase:

PHASE4

Brief Summary

Chronic Obstructive Pulmonary Disease (COPD) is a major worldwide problem.Steroids inhalers are now an established treatment for COPD. Inhaled steroids can have a number of bad effects including suppr...

Eligibility Criteria

Inclusion

  • Current or ex-smokers
  • Aged over 50years
  • FEV1/FVC ratio \<0.7
  • FEV1\<80% predicted
  • Improvement in FEV1 following short acting beta-agonist not greater than 15% and 200ml.

Exclusion

  • Diagnosis of asthma, bronchiectasis or ABPA
  • Inability to perform study procedures or give informed consent
  • Known sensitivity to trial medications

Key Trial Info

Start Date :

October 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2008

Estimated Enrollment :

18 Patients enrolled

Trial Details

Trial ID

NCT00995475

Start Date

October 1 2006

End Date

November 1 2008

Last Update

May 19 2023

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