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This study plans to learn more about specific breathing and activity recommendations for patients after surgery. Participants will be monitored after abdominal surgery to identify what activities help them breathe better and reduce complications after surgery.
Investigators will study adults undergoing elective abdominal surgery with at least moderate risk for postoperative pulmonary complications. Participants will be monitored on their chest and thigh with devices that record their breathing pattern (breath volume and frequency) and body position and movements. These monitors will be placed on their skin in the Post-Anesthesia Care Unit (PACU) and will stay on for three days, or until the patient is able to ambulate freely or until their hospital discharge, whichever comes earlier. Investigators will analyze the association between the frequency, duration and intensity of various activities (e.g., sitting, walking) and breathing and other clinical complications, in combination with medications received and other hospital course events.
Age
18 - 90 years
Sex
ALL
Healthy Volunteers
No
UC Health
Aurora, Colorado, United States
Start Date
December 22, 2022
Primary Completion Date
December 22, 2025
Completion Date
June 22, 2026
Last Updated
April 30, 2025
30
ESTIMATED participants
ExSpiron and ActivPAL Monitors
DEVICE
Lead Sponsor
University of Colorado, Denver
Collaborators
NCT07186933
NCT06169514
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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