Postoperative Respiratory and Activity Monitoring
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorUniversity of Colorado, Denver
About this trial
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.
Eligibility criteria
Qualifiers
Must be 18 or older
Must be undergoing abdominal surgery
Must be high-risk for PPCs (ARISCAT score equal to or greater than 26)
Disqualifiers
Anyone under 18
Anyone not undergoing abdominal surgery
Anyone that is not high-risk for PPCs (ARISCAT score less than 26)
Trial design
Treatments tested in this trial
- ExSpiron and ActivPAL Monitors
Treatment groups
30 Participants
are divided into 1 treatment groupSponsors and collaborators
University of Colorado, Denver
Lead sponsor
Brigham and Women's Hospital
Collaborator
Source ClinicalTrials.gov