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Clinical Trial Summary

To determine the efficacy of oscillatory positive expiratory pressure (OPEP) therapy on patients admitted through the trauma service line for rib fractures, as compared to incentive spirometry (IS).


Clinical Trial Description

Patients identified through screening procedures to fit the inclusion criteria will be approached, within 48 hours of floor admission, to participate in the study. Once written informed consent is obtained, participants will be randomized, in a 1:1 ratio, into either the IS or OPEP study group. Each patient will be instructed on how to use the respiratory therapy device, either IS or OPEP, by research personnel and respiratory therapists. Participants will be instructed to record their compliance with the RT protocol in their respective patient diaries. Respiratory Therapy will record FVC three times daily on all study participants until stable (FVC > 1.5L x 4), then daily for up to 7 days or until discharge. Participants will be contacted on day 30 from discharge, and administered a short questionnaire. All participants will be followed and monitored per standard of care, under the care and supervision of their treating provider teams. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04100512
Study type Interventional
Source Poudre Valley Health System
Contact Julie Dunn, MD
Phone 970.624.1689
Email julie.dunn@uchealth.org
Status Recruiting
Phase N/A
Start date October 21, 2019
Completion date October 31, 2023

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