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RECRUITING
NCT05565495
PHASE2

The Effects of ECMO on the Pharmacokinetics of Hydromorphone

Sponsor: Xiaobo Yang, MD

View on ClinicalTrials.gov

Summary

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 Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

26

Start Date

2022-01-01

Completion Date

2024-09-01

Last Updated

2024-08-06

Healthy Volunteers

No

Interventions

DRUG

Hydromorphone

Hydromorphone was administered intravenously at a rate of 0.03 mg/kg/h for 72 h for analgesia. Blood samples were collected before administration and at different time points after administration, and the contents of hydromorphone and hydromorphone-3-glucuronide (main metabolite) were detected by quantitative liquid chromatography tandem mass spectrometry, and then A population pharmacokinetic model of hydromorphone in patients under ECMO was established.

Locations (1)

Wuhan Union Hospital

Wuhan, Hubei, China