Timing of Opioid Administration and Postoperative Respiratory Depression.
Recruiting
Observational Study
Respiratory Complications
Opioid Induced Respiratory Depression
Postoperative Respiratory Complications
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 85
- Sex
- Any
- Study type
- Observational
- Participants needed
- 52 (estimated)
- Sponsor
- Wayne State University · Other
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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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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
Exclusion Criteria:
* Non-operative procedure …
Contacts