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Population pharmacokinetic study of Remimazolam in critically ill patients with VA-ECMO

Population pharmacokinetic study of Remimazolam in critically ill patients with VA-ECMO

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063047
Enrollment
Unknown
Registered
2022-08-29
Start date
2022-08-30
Completion date
Unknown
Last updated
2023-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiogenic shock

Interventions

Group 1:Venous continuous pump injection of Remimazolam

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Over 18 years old; 2. Patients who meet the indications and receive VA-ECMO therapy for more than 24 hours of invasive mechanical ventilation.

Exclusion criteria

Exclusion criteria: 1. Known hypersensitivity to remimazolam tosylate, taking any drug that may cause drug-drug interaction or change the concentration of remimazolam tosylate; 2. Patients with severe kidney disease in the past, chronic kidney disease history of more than 4 stages or dialysis or preoperative estimated glomerular filtration rate < 30 ml/min.

Design outcomes

Primary

MeasureTime frame
Pharmacokinetics;

Secondary

MeasureTime frame
General basic patient information;ECMO duration;Serum creatinine;Plasma pH;

Countries

China

Contacts

Public ContactFen Liu

The First Affiliated Hospital of Nanchang University

dengwei1992868@163.com+86 19884340796

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026