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Documentation of specific indications of lipoprotein apheresis - Real World Study

Documentation of specific indications of lipoprotein apheresis - Real World Study - RWS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00011704
Enrollment
100
Registered
2017-02-09
Start date
2017-02-15
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

E78.0 G60.1 E78.1 E78.2 E78.3 E78.4 E78.5 E78.8 E78.9

Interventions

Group 1: The data of patients with the indication of lipoprotein apheresis are documented: Retrospective part: • Before the onset of lipoprotein apheresis treatment
(e.g., lipid parameters, mutations, first cardiovascular manifestations, or other disease-specific manifestations and symptoms, events and interventions, relevant adjunctive diseases, medication). Pr

Sponsors

Apherese Forschungsinstitut
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: In the case of the patients examined in the context of this documentation, the indication for lipoprotein apheresis exists. The patients covered in this documentation are routinely treated within the contractual medical care of lipoprotein apheresis. General inclusion / exclusion criteria: • The respondent is in a position to give his / her informed consent to study participation after elucidation. • Male and female subjects, age = 18 years.

Exclusion criteria

Exclusion criteria: The following criteria lead to the exclusion / withdrawal of the study for the person concerned: • The subject withdraws his consent. • Any medical or non-medical reason which, in the opinion of the examiner, requires the completion of the documentation for the subject. • The investigation can be terminated at the beginning at any time by the sponsor or the director of the documentation.

Design outcomes

Primary

MeasureTime frame
Documentation of the efficacy of lipoprotein apheresis in different indications; Clinical and laboratory parameters.

Secondary

MeasureTime frame
• Effectiveness of lipoprotein apheresis by clinical parameters (e.g., occurrence of cardiovascular events, course of disease-specific symptoms) • Documentation of safety and tolerability using reference apheresis treatments • documentation of disease-specific laboratory parameters before, during and after therapy (e.g., LDL cholesterol, lipoprotein(a), triglycerides)

Countries

Germany

Contacts

Public ContactReinhard Klingel

Apherese Forschungsinstitut

afi@apheresis-research.org+49 221 4063170

Outcome results

None listed

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