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UnknownNCT03948880

Incidence OIRD Medical and Trauma Patients

Incidence of OIRD in Medical and Trauma Patients on the General Care Floor Receiving PCA or Nurse Administered Intravenous Opioids Monitored by Capnography and Pulse Oximetry: A Prospective, Blinded Observational Study

Status
Unknown
Phase
Study type
Observational
Enrollment
101 (estimated)
Sponsor
Community Health System · Academic / Other
Sex
All
Age
18 Years – 89 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this prospective, blinded observational study is to correlate assessment of sedation and respiratory status with capnography and pulse oximetry monitoring in hospitalized adult medical and trauma patients receiving patient-controlled analgesia (PCA) or nurse administered intravenous opioids for acute pain. Nursing assessment of respiratory status and sedation level will be correlated with capnography and pulse oximetry values as technology-supported monitoring to identify respiratory depression and opioid-induced sedation. The secondary objective is to identify capnography and pulse oximetry values that correlate with respiratory decompensation and opioid-induced sedation in medical and trauma patients on the general care floor.

Conditions

Timeline

Start date
2019-07-29
Primary completion
2019-10-29
Completion
2019-11-29
First posted
2019-05-14
Last updated
2019-07-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03948880. Inclusion in this directory is not an endorsement.

Incidence OIRD Medical and Trauma Patients (NCT03948880) · Clinical Trials Directory