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Effects of IPV Assessed With Functional Imaging

A

Antwerp University Hospital (UZA)

Status

Unknown

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Device: intrapulmonary percussive ventilation
Other: standard treatment

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01671540
PML_Kine_IPV
artesis_G018 (Other Identifier)

Details and patient eligibility

About

In this study the invetigators seek an answer on the following hypothesis:

  • What are the long term effects of an IPV treatment evaluated with classical outcome parameters? (FEV1, Raw)
  • Is the possible effect noticeable on the novel technique and is this comparable with the classical outcome parameters?

Full description

A Multicenter study conducted in university Hospital Antwerp (UZA) and ZNA Middelheim.

Tests are taken before and after one week IPV treatment. IPV is applied for 1 week during the physical therapy treatment of chronic obstructive pulmonary desease (COPD) patients admitted to the hospital for an excarebation. The IPV treatment is an additional treatment upon the standard treatment of the patients. The standard treatment consists out of existing drainage techniques to remove secretion out of the lungs by means of breathing control exercises. Patients are randomized into either the experimental group or the control group. The control group receives a standard physical therapy treatment without additional IPV treatment.

Enrollment

20 estimated patients

Sex

All

Ages

30+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients admitted in the hospital for a acute exacerbation
  • Mild to severe COPD

Exclusion criteria

  • Ischemic / ventricular aritmic
  • Tracheotomise
  • Pneumothorax
  • Facial deformity
  • Recent nose, mouth or ear operations
  • Recent gastric operations.
  • Intubated
  • Epilepsy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Triple Blind

20 participants in 2 patient groups

Intrapulmonary percussive ventilation
Experimental group
Description:
IPV is applied for 1 week (once a day) during the physical therapy treatment of the patient
Treatment:
Device: intrapulmonary percussive ventilation
standard airwy claerance regime
Active Comparator group
Description:
The standard treatment consists out of existing drainage techniques to remove secretion out of the lungs by means of breathing control exercises
Treatment:
Other: standard treatment

Trial contacts and locations

1

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Central trial contact

Kris Ides, Msc

Data sourced from clinicaltrials.gov

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