Title

Erdosteine (Erdotin) Versus Standard Care Plus Placebo on Erdosteine for Treatment of Cough in Acute Exacerbations of Chronic Obstructive Pulmonary Disease (COPD)
A Double Blind, Placebo Controlled Multicentre Study of the Effects of Standard Care Plus Erdosteine (Erdotin) Versus Standard Care Plus Placebo on Cough in Acute Exacerbations of Chronic Obstructive Pulmonary Disease (COPD)
  • Phase

    Phase 4
  • Study Type

    Interventional
  • Status

    Withdrawn
  • Intervention/Treatment

    erdosteine ...
  • Study Participants

    0
This is a parallel group, double-blind, placebo controlled, multi-centre, randomised trial.

60 patients to be included who are adult patients admitted to hospital with a clinical diagnosis of acute exacerbation of Chronic Obstructive Pulmonary Disease (COPD). Acute exacerbation of COPD will be defined as sustained worsening of the patient's condition with an increase in cough and one or more of dyspnoea, sputum volume or sputum purulence, necessitating a change in regular medication.

The primary objective of this study is to evaluate the effectiveness of standard care plus erdosteine in reducing hourly cough (24 hour cough recording using automated cough recorder) measured from baseline (Day 0) and at Day 5 of treatment, compared with standard care plus placebo.
Study Started
Aug 10
2010
Anticipated
Primary Completion
Oct 12
2011
Anticipated
Study Completion
Jan 13
2012
Anticipated
Last Update
Jun 19
2019

Drug Erdosteine

capsule 300mg twice daily for 10 days

  • Other names: erdotin

Drug Placebo

placebo capsule, twice daily for 10 days

erdosteine Experimental

standard care plus erdosteine for 10 days

placebo Placebo Comparator

Standard care for exacerbation of COPD plus placebo

Criteria

Inclusion Criteria:

Male/females aged between 40-80 years
Previous diagnosis of COPD
Acute exacerbation of COPD requiring treatment with antibiotics and/or corticosteroids
Symptoms of increased breathlessness, cough, sputum volume or sputum purulence
Acute exacerbation of COPD hospitalised within 24hrs of study participation.
On a stable therapeutic regimen for COPD for 8 weeks prior to inclusion
Known history of cigarette smoking at least 10 pack yrs
Willing and able to comply with study procedures
Able to provide written informed consent to participate

Exclusion Criteria:

Acute exacerbation of COPD within 8 weeks prior to inclusion
Arterial blood gas on admission < pH 7.26
Currently on treatment with mucolytics
Patients suffering from post nasal drip, or gastro-oesophageal reflux disease
Clinically significant or unstable concurrent disease e.g. left ventricular failure, diabetes mellitus
On long-term oxygen therapy
Known or suspected hypersensitivity to erdosteine
No Results Posted