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Evaluation of High-Frequency Chest Wall Oscillation

H

Hill-Rom

Status

Completed

Conditions

Airway Secretion Clearance

Treatments

Device: Airway clearance Device

Study type

Interventional

Funder types

Industry

Identifiers

NCT00717873
CR-0080

Details and patient eligibility

About

To compare the outcomes of patients treated with the Vest and conventional chest physiotherapy to determine if the Vest provides equivalent therapy

Enrollment

105 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Acute or chronic disease requiring secretion mobilization as per hospital protocol

Exclusion criteria

  • Absolute contraindications for positional changes
  • Absolute contraindications for chest percussion
  • Women visibly pregnant
  • Previous enrollment in study
  • Previous CPT or Vest treatment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

105 participants in 2 patient groups

HFCWO Arm
Experimental group
Description:
Airway clearance provided by the Vest Airway Clearance System
Treatment:
Device: Airway clearance Device
CPT Arm
No Intervention group
Description:
Airway clearance provided by manual CPT

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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