Clinical Trials Directory

Trials / Completed

CompletedNCT01480882

Efficacy and Safety Study of a Percussion Device to Mobilise Sputum From Respiratory Passage

"A Prospective, Cross-over Randomized Trial to Assess the Efficacy and Safety of Mechanical Percussor "LEGA" Compared With Conventional Chest Physiotherapy in Adults With Chronic Bronchiectasis or Chronic Obstructive Pulmonary Disease (COPD

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Penang Hospital, Malaysia · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

A Malaysian company by name Formedic Technologies SDN BHD has devised a hand held machine which is supposed to mimic the chest percussion performed by professional physiotherapist to mobilize sputum through the respiratory passage. The aim of this study is to compare the effectiveness and safety of this mechanical percussion device in the treatment of airway clearance with conventional chest physiotherapy carried out by qualified physiotherapists in patients suffering from bronchiectasis or Chronic obstructive Pulmonary disease (COPD).

Detailed description

This study will compare the amount of sputum expectorated during the two procedures and not intended to look at the clinical improvement of the patient.

Conditions

Interventions

TypeNameDescription
PROCEDUREConventional Chest Physiotherapy (CCPT)Conventional chest percussion will be applied for a duration of 15 minutes.
DEVICEMechanical percussion (LEGA)Mechanical chest percussion will be delivered by a device for 15 minutes.

Timeline

Start date
2011-12-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2011-11-29
Last updated
2012-12-06

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT01480882. Inclusion in this directory is not an endorsement.