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The efficacy of lipoprotein(a) removal by lipoprotein apheresis in patients with hyperlipoprotein(a)

The efficacy of lipoprotein(a) removal by lipoprotein apheresis in patients with hyperlipoprotein(a)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260708005
Enrollment
5
Registered
2026-07-08
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

hyperlipoprotein(a) Hyperlipoprotein(a) Lipid apheresis lipoprotein(a)

Interventions

Lipid apheresis will be done at day 0, 14, 28 and patients will be further follow up for a total of 42 days. Technique used will be double filtration plasmapheresis using Plasauto-Sigma machine (Asahi
Experimental Device

Sponsors

Faculty of Medicine Siriraj Hospital, Mahidol University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult (aged > 18-70 years old) patients with 1. Lp(a) more than 200 nmol/L or 2. Lp(a) more than 125 nmol/L (estimated around 60 mg/dL) and having ASCVD or having high risk for atherosclerosis cardiovascular disease (defined as Thai CV risk more than or equals to 20%)

Exclusion criteria

Exclusion criteria: 1. Having contraindication of heparin use such as hypersensitivity to heparin, history of heparin induced thrombocytopenia, active or uncontrolled bleeding, platelet count < 100,000/mm3 , coagulopathy 2. Recent ASCVD or major surgery within 3 months 3. Receiving PCSK9 inhibitor 4. Having terminal illness 5. Cannot provide consent by themselves 6. History of allergy or reactions to the dialyzers 7. Hypocalcemia (serum total calcium, corrected with albumin < 8.5 mg/dL) on the morning of scheduled LA 8. Hypokalemia (serum potassium < 3.0 mmol/L) on the morning of scheduled LA 9. Hypomagnesemia (serum magnesium < 1.6 mg/dL) on the morning of scheduled LA 10. Severe anemia (Hct <25%)

Design outcomes

Primary

MeasureTime frame
Efficacy Day 0, 3, 7, 14, 28, 42 serum Lp(a) level, total cholesterol, HDL-cholesterol, direct LDL-cholesterol, triglyceride, hsCRP

Secondary

MeasureTime frame
Safety day 0, 14, 28 Adverse events (vascular access AE, DFPP related AE), serum calcium, PT/APTT, fibrinogen

Countries

Thailand

Contacts

Public ContactNuntakorn Thongtang

Faculty of Medicine Siriraj Hospital, Mahidol University

nuntakorn.thn@mahidol.ac.th024197799

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026