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The effect of different plasma infusion method on coagulation factors in double filtration plasmapheresis, a pilot study

The effect of different plasma infusion method on coagulation factors in double filtration plasmapheresis, a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083663
Enrollment
Unknown
Registered
2024-04-30
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Blood purification

Interventions

Experimental group:Plasma transfusion after DFPP treatment
Control group:Supplementing plasma during DFPP treatment

Sponsors

Shanghai East Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1: Requiring DFPP treatment for any reason 2: Requiring the use of Cascadeflo EC 20W as a secondary plasma separator due to clinical necessity 3: No severe organic or psychiatric disorders 4: Patients who understand and are willing to cooperate with this study and consent to participate by signing an informed consent form

Exclusion criteria

Exclusion criteria: 1: Age less than 18 years or older than 80 years 2: Pregnant or lactating 3: Presence of contraindications to heparin 4: Presence of thrombocytopenia (PLT < 100 * 10^9/L) 5: Presence of significant bleeding risk 6: Severe liver dysfunction 7: Inability to establish suitable vascular access 8: Refractory shock 9: End-stage malignant tumors 10: Expected survival time < 48 hours 11: Lack of legal capacity

Design outcomes

Primary

MeasureTime frame
Coagulation factor activity;

Secondary

MeasureTime frame
APTT;PT;INR;Platelets;

Countries

China

Contacts

Public ContactZhang Yunhe

Shanghai East Hospital

zyhe31@163.com+86 139 1790 8722

Outcome results

None listed

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