Trials / Terminated
TerminatedNCT00279097
Safety Study to Evaluate Intracranial Pressure During High Frequency Chest Wall Oscillation
A Safety Study to Evaluate Intracranial Pressure With the Utilization of High Frequency Chest Wall Oscillation (HFCWO) Using the Vest™ on Mechanically Ventilated Neurosurgical Patients
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (planned)
- Sponsor
- Hill-Rom · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate changes in intracranial pressure (ICP) during or immediately following high frequency chest wall oscillation (HFCWO) treatment with the Vest™ in neurosurgical subjects.
Detailed description
This study is a single site safety study to evaluate changes in intracranial pressure during or immediately following HFCWO treatment with the Vest™ in neurosurgical subjects with intracranial pressure monitors having normal opening pressures and ICP less than or equal to 20 mmHg. The secondary objective of this study is to evaluate changes in arterial blood gases that may result with Vest™ therapy in ventilated patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | High Frequency Chest Wall Oscillation |
Timeline
- Start date
- 2006-01-01
- Completion
- 2006-09-01
- First posted
- 2006-01-19
- Last updated
- 2006-11-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00279097. Inclusion in this directory is not an endorsement.