The Effects of ECMO on the Pharmacokinetics of Hydromorphone
Recruiting now · Phase 2
Conditions studied: Extracorporeal Membrane Oxygenation
In brief
The purpose of this study was to establish a population pharmacokinetic (PPK) model of hydromorphone in patients under ECMO, and to recommend a dosing regimen when the target effective concentration was reached.
Key facts
- Study ID
- NCT05565495
- Run by
- Xiaobo Yang, MD
- People needed
- 26
- Starts
- 2022-01-01
- Expected to finish
- 2024-09-01
- Last updated by the study team
- 2024-08-06
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Between the ages of 18 and 80;
- Using hydromorphone for pain relief;
- Using ECMO for more than 96h
You may not qualify if…
- Allergic to hydromorphone;
- Use of CRRT during ECMO;
- Liver function Child-Pugh B, C grade;
- Pregnancy;
- Intestinal obstruction;
- Refused to sign the informed consent.
Where it is running
- Wuhan Union Hospital — Wuhan, Hubei, China (enrolling)
Full record on ClinicalTrials.gov
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