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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01046175
Other study ID # S-09326b
Secondary ID
Status Withdrawn
Phase Phase 2
First received December 22, 2009
Last updated November 11, 2010
Start date February 2010
Est. completion date June 2011

Study information

Verified date December 2009
Source Ullevaal University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway:National Committee for Medical and Health Research Ethics
Study type Interventional

Clinical Trial Summary

Respiratory complications continue to be one of the leading causes of morbidity and mortality in people with spinal cord injury, especially among cervical and higher thoracic injuries. Both inspiratory and expiratory function are often severely decreased, leading to respiratory complications, such as atelectasis, pneumonia and ventilatory failure. The prevention of these respiratory complications needs to begin immediately after injury. To achieve effective expelling of secretions before they form mucus plugs, it is essential to improve patients ability to cough. Manually assisting the cough is one way of increasing cough flow, but an effective cough also requires adequate lung volumes. The emphasis should therefore be on expansion of the lungs before coughing. One way of expanding the lungs is by air-stacking. In air-stacking insufflations are stacked in the lungs to maximally expand them. Cough can be valued by measuring Peak Cough Flow (PCF). By combining air-stacking with manually assisted cough the PCF can be increased sufficiently. The aim of this study is to compare the effect of two different air-stacking techniques on PCF, air-stacking on a respirator versus air-stacking with a manual resuscitator.


Recruitment information / eligibility

Status Withdrawn
Enrollment 10
Est. completion date June 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- acute cervical or high thoracic spinal cord injury admitted to the ICU

Exclusion Criteria:

- substantial abdominal or thoracic injury

- substantial brain damage

- intubated or tracheostomized patients

- not able to cooperate

- pregnant women

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Air-stacking with a manual resuscitator
Stacking air into the lungs up to maximal insufflation capacity (MIC)with a manual resuscitator
Air-stacking with ventilator
Stacking air into the lungs to maximal insufflation capacity (MIC) with ventilator

Locations

Country Name City State
Norway Oslo University Hospital, Ullevaal Oslo

Sponsors (1)

Lead Sponsor Collaborator
Ullevaal University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peak cough flow (PCF) 2 weeks No
Secondary Patient preference of air-stacking technique 2 weeks No
Secondary Physiotherapist preference of air-stacking technique 2 weeks No
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