Expired Study
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St. Louis, Missouri 63110


Purpose:

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


Criteria:

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


NCT ID:

NCT00717873


Primary Contact:

Principal Investigator
Darnetta Clinkscale, RRT
Barnes-Jewish Hospital Foundation


Backup Contact:

N/A


Location Contact:

St. Louis, Missouri 63110
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 16, 2018

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