Timing of Opioid Administration and Postoperative Respiratory Depression.

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorWayne State University

About this trial

The goal of this study is to determine if a relationship can be detected between the administration of an opioid and quantitative respiratory depression in spontaneously breathing non-intubated patients who have undergone general anesthesia and have received perioperative opioids.

The primary aim is to determine the temporal effect of opioid administration on respiratory depression as assessed by minute ventilation with a reduction of at least 20% in the percent of predicted minute ventilation.

A secondary aim is to determine a dose response of opioid administration and its effect on minute ventilation.

The investigators aim to determine the influence of opioid administration on minute ventilation on spontaneously breathing patients during post-anesthesia care unit (PACU) stay.

Eligibility criteria

Qualifiers

Written informed consent

Adults ≥18 years of age and ≤85 years of age

Patients planned for general anesthesia with an expected anesthetic time of at least 2 hours

Patients expected to receive postoperative opioid analgesia

Disqualifiers

Non-operative procedure (imaging)

Patients not admitted to the PACU postoperatively

Use of patient-controlled analgesia systems

Female patients who are pregnant or breastfeeding

Trial design

Treatments tested in this trial

  • Respiratory volume monitoring

Treatment groups

52 Participants
are divided into 1 treatment group

Sponsors and collaborators