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Comparison of safety and efficacy of different therapeutic doses of DPMAS

Comparison of safety and efficacy of different therapeutic doses of DPMAS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070112
Enrollment
Unknown
Registered
2023-04-03
Start date
2023-04-03
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Severe liver failure

Interventions

The 3h treatment group:3h therapeutic dose
The 4h treatment group:4h therapeutic dose
The 5h treatment group:5h therapeutic dose

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: ? The patients with liver failure admitted to West China Hospital of Sichuan University meet the indications of artificial liver therapy stipulated in Expert Consensus on Clinical Application of Artificial Liver Blood Purification Technology (2022 Edition), that is, "patients with pre-, early-stage, mid-stage and late-stage liver failure caused by various causes;Patients with end-stage liver disease waiting for liver source before liver transplantation, rejection after liver transplantation, and non-functional liver transplantation;Patients with severe cholestatic liver disease and severe hyperbilirubinemia caused by various causes;Other diseases, such as sepsis with severe liver injury or multiple organ dysfunction syndrome, acute poisoning, etc. "? Age 18-70 years old;? Total bilirubin >200umol/L;? Stable hemodynamics and tolerance to artificial liver therapy;? The patient agrees and signs the informed consent voluntarily.

Exclusion criteria

Exclusion criteria: ? Hemodynamic instability (blood pressure <90/60mmHg);? Mental illness or other reasons can not cooperate with treatment;? Patients with severe active bleeding or disseminated intravascular coagulation; ? Allergic to consumables, blood products or drugs used in the treatment;? The same patient was only included in one DPMAS treatment, and the researchers who had participated in this study were no longer included;? Other researchers think it is not suitable to participate in the study.

Design outcomes

Primary

MeasureTime frame
Total bilirubin;

Secondary

MeasureTime frame
Inflammatory factor;

Countries

China

Contacts

Public ContactYingying Yang

West China Hospital, Sichuan University

yingyingyangsf@163.com13688398045

Outcome results

None listed

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