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

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

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 Discharge

an average of 10 days

Outcome measures

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

Darnetta Clinkscale

Barnes Jewish Hospital

Phone: (314) 362-1276

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place