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Timing of Opioid Administration and Postoperative Respiratory Depression.

NCT07227389

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Respiratory Complications
  • Opioid Induced Respiratory Depression
  • Postoperative Respiratory Complications

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 to 85 years
Sex
All
Healthy volunteers
Accepted
Sponsor
Wayne State University
Last updated on ClinicalTrials.gov
July 16, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Michigan · 1

  • Detroit Medical Center · Detroit, MI

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.