Trial Outcomes & Findings for Evaluation of High-Frequency Chest Wall Oscillation (NCT NCT00717873)
NCT ID: NCT00717873
Last Updated: 2017-08-07
Results Overview
an average of 10 days
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
105 participants
Primary outcome timeframe
Admission to Discharge
Results posted on
2017-08-07
Participant Flow
Participant milestones
| Measure |
HFCWO Arm
Airway clearance provided by the Vest Airway Clearance System
|
CPT Arm
Airway clearance provided by manual CPT
|
|---|---|---|
|
Overall Study
STARTED
|
46
|
59
|
|
Overall Study
COMPLETED
|
46
|
59
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Evaluation of High-Frequency Chest Wall Oscillation
Baseline characteristics by cohort
| Measure |
HFCWO Arm
n=46 Participants
Airway clearance provided by the Vest Airway Clearance System
|
CPT Arm
n=59 Participants
Airway clearance provided by manual CPT
|
Total
n=105 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
42 years
STANDARD_DEVIATION 18 • n=5 Participants
|
45 years
STANDARD_DEVIATION 18 • n=7 Participants
|
44 years
STANDARD_DEVIATION 18 • n=5 Participants
|
|
Sex: Female, Male
Female
|
17 Participants
n=5 Participants
|
33 Participants
n=7 Participants
|
50 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
29 Participants
n=5 Participants
|
26 Participants
n=7 Participants
|
55 Participants
n=5 Participants
|
PRIMARY outcome
Timeframe: Admission to Dischargean average of 10 days
Outcome measures
| Measure |
HFCWO Arm
n=46 Participants
Airway clearance provided by the Vest Airway Clearance System
|
CPT Arm
n=59 Participants
Airway clearance provided by manual CPT
|
|---|---|---|
|
Hospital Length of Stay
|
2.95 days
Standard Deviation 1.01
|
5.45 days
Standard Deviation 1.84
|
Adverse Events
HFCWO Arm
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
CPT Arm
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place