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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02140892
Other study ID # SHEBA-13-0697-YO-CTIL
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 14, 2014
Last updated May 15, 2014
Start date July 2014
Est. completion date December 2015

Study information

Verified date May 2014
Source Sheba Medical Center
Contact Yaakov (kobi) Dagan, Msc.
Phone 0523694979
Email kobi.dagan@sheba.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

One of the main goals of the respiratory physical therapy is to help people who are suffering from accumulating of secretions in their airways and lungs.

Chronic Obstructive Pulmonary Disease (COPD) patients are often hospitalized with an Acute Exacerbation of their medical condition.

Those patients usually get only the standard medical care during the acute phase and don't get respiratory physical therapy treatment.

The study's main aim is to investigate if respiratory physical therapy treatment in addition to standard medical care during the acute phase, can improve the respiratory and medical condition and reduce hospitalization stay.

In order to do so we will compare three groups of COPD patients during acute exacerbation; two groups will get one out of two respiratory physical therapy techniques; manually or Intrapulmonary Percussive Ventilator (IPV) in addition to standard medical care and the third group will get standard medical care alone.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 75
Est. completion date December 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender Both
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

- clinical diagnosis of Acute Exacerbation of COPD or Acute Exacerbation of Chronic Bronchitis

- Respiratory Rate>25

- PaCO2> 45 mmHg

- 7.35 < PH < 7.38

Exclusion Criteria:

- intubation

- apnea

- glasgow coma scale < 8

- pneumothorax

- FEV1 < 50% predicted

- Ischemic Hearth Disease

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
respiratory physical therapy manual technique- Autogenic Drainage

Device:
respiratory physical therapy technique- IPV


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary length of stay in the hospital up to three months No
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