Effect of high-frequency chest wall oscillation and manual hyperinflation on the resolution of atelectasis in ventilated patients

Effect of high-frequency chest wall oscillation and manual hyperinflation on the resolution of atelectasis in ventilated patients - Oscillation or manual hyperinflation

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON30499

Enrollment

Registered

2007-01-29

Start date

2007-03-01

Completion date

Unknown

Last updated

2024-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

atelectasis mucusplug

Interventions

Patients who meets the entry criteria and agree to participate in the study will be split up by randomisation. 10 Patients will be the intervention group and treaded with The Vest* therapy and 10 pa

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: patients older than 18 years Atelectasis visible radiographically Informed consent

Exclusion criteria

Exclusion criteria: Patients with coagulationproblems Patients with cancer and metastasis in the thorax area Patients with spinal column fracture Patients with spinal cord injury Patients with recent rib fracture Patients with high intracerebal pressure Patients who are bleeding Patients with open wounds at the thoracal area Patients with thoraxtubes Restless patients

Design outcomes

Primary

Measure	Time frame
Primary study parameters are: age sex primary diagnosis APACHE-score Ventilator-mode FiO2 Inspir./ expir. relation mandatory breaths Expired minute volume and tidal volume Peak airway pressure positive end-expiratiore pressure SaO2 PeCO2 Dynamic compliance Mean art. pressure (MAP) Hartrate bodytemperature suction frequency x-ray diagnosis bronchoscopic suction transfer to an other unit Leukocyte count * use of antibiotics Measuringmoments: o T-0 = 1th measuringmoment, immediately before start intervention o T-1 = 2th measuringmoment, immediately after finish intervention o T-2 = 3th measuringmoment, 1 hour after intervention	—

Measure

Time frame

Primary study parameters are: *age *sex *primary diagnosis *APACHE-score *Ventilator-mode *FiO2 *Inspir./ expir. relation *mandatory breaths *Expired minute volume and tidal volume *Peak airway pressure *positive end-expiratiore pressure *SaO2 *PeCO2 *Dynamic compliance *Mean art. pressure (MAP) *Hartrate *bodytemperature *suction frequency *x-ray diagnosis *bronchoscopic suction *transfer to an other unit *Leukocyte count * use of antibiotics Measuringmoments: o T-0 = 1th measuringmoment, immediately before start intervention o T-1 = 2th measuringmoment, immediately after finish intervention o T-2 = 3th measuringmoment, 1 hour after intervention

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Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)