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Effect of different precharging modalities on the treatment of moderate hypotension with DPMAS: a single-center randomized controlled study

Effect of different precharging modalities on the treatment of moderate hypotension with DPMAS: a single-center randomized controlled study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080997
Enrollment
Unknown
Registered
2024-02-20
Start date
2024-02-22
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Liver failure

Interventions

Intervention group:1000ml amber gel injection was used to pre-flush the DPMAS extracorporeal circulation pipeline, and the blood pressure was measured by a wall-mounted multifunctional monitor in the
Control group:1000ml normal saline was used to pre-flush the DPMAS extracorporeal circulation pipeline, blood pressure was measured by a wall-mounted multi-functional monitor in the ICU. The blood pr

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ?Patients with liver failure admitted to West China Hospital of Sichuan University meet the indications for the treatment of artificial liver prescribed in the Expert Consensus on the Clinical Application of artificial liver Blood Purification Technology (2022 edition), that is, "patients with pre-liver failure, early, middle and late liver failure caused by various reasons; 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. "? Patients with stable hemodynamics before DPMAS treatment (blood pressure > 90/60mmHg); ? The patient agrees and voluntarily signs the informed consent; ?Age =18 years old

Exclusion criteria

Exclusion criteria: ? Mental illness or other reasons can not cooperate with treatment; ? Female pregnancy test positive (pregnant women); ? Patients who have participated in other studies; ? Patients receiving other artificial liver treatment regimens; ? People with a history of allergy to succinyl gelatin injection, consumables used, blood products or drugs

Design outcomes

Primary

MeasureTime frame
Number and incidence of hypotension;

Secondary

MeasureTime frame
Adverse events: allergic reactions, arrhythmia, bleeding, number of rescue cases, adjustment of vasopressor medication, etc;

Countries

China

Contacts

Public ContactLin Li

West China Hospital of Sichuan University

932061196@qq.com+86 139 8202 5375

Outcome results

None listed

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