NCT01480882View on ClinicalTrials.gov

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

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

December 31, 2011

Primary Completion Date

June 30, 2012

Study Completion Date

June 30, 2012

Conditions
Chronic BronchiectasisChronic Obstructive Pulmonary Disease (COPD)
Interventions
PROCEDURE

Conventional Chest Physiotherapy (CCPT)

Conventional chest percussion will be applied for a duration of 15 minutes.

DEVICE

Mechanical percussion (LEGA)

Mechanical chest percussion will be delivered by a device for 15 minutes.

Trial Locations (1)

10990

Penang hospital, George Town

All Listed Sponsors
lead

Penang Hospital, Malaysia

OTHER_GOV

NCT01480882 - Efficacy and Safety Study of a Percussion Device to Mobilise Sputum From Respiratory Passage | Biotech Hunter | Biotech Hunter