Status:
COMPLETED
Comparison of the Plasma Lipoprotein Apheresis Systems DIAMED and MONET vs. the Whole Blood Apheresis System DALI
Lead Sponsor:
Fresenius Medical Care Deutschland GmbH
Conditions:
Hypercholesterolemia, Familial
Dyslipidemias
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The clinical Investigation will be performed to compare the safety and effectiveness of the CE certified and established lipoprotein apheresis systems MONET vs. DALI and DIAMED vs. DALI for optimizing...
Detailed Description
Comparison of the safety and effectiveness of the CE certified and established lipoprotein apheresis systems MONET vs. DALI and DIAMED vs. DALI for optimizing the individual therapy of patients with s...
Eligibility Criteria
Inclusion
- Informed consent signed and dated by study patient and investigator/authorised physician
- Minimum age of 18 years
- Ability to understand the nature and requirements of the study
- Study-specific inclusion criteria:
- Patients with indication for lipoprotein apheresis confirmed by a local apheresis expert commission according to the German guidelines \[1\] and with routine lipoprotein apheresis treatments for at least 3 months. Patients with weekly treatments have not missed more than 3 treatment sessions within the 3 months prior inclusion to the study. Patients with biweekly treatment sessions have not missed more than 1 treatment session within the 3 months prior inclusion to the study
- Patients with regular weekly or biweekly lipoprotein apheresis treatments with either MONET or DIAMED lipoprotein apheresis systems for at least 4 weeks (weekly treatments) or 8 weeks (biweekly treatments) with the same system
- With adequate venous access
- With systolic blood pressure \> 100 mmHg
- With stable hematocrit \>35 %
- With stable anticoagulation
Exclusion
- Any condition which could interfere with the patient's ability to comply with the study
- Pregnancy or lactation period (pregnancy test will be conducted with female patients aged 55 years)
- Participation in an interventional clinical study during the preceding 30 days or in the same study
- Study-specific exclusion criteria:
- Occurrence or clinical relevant deterioration of acute myocardial infarction, unstable angina pectoris, severe hemo-dynamic relevant arrhythmia within 3 months prior inclusion to the study
- Bypass surgery, vascular diseases, active infection (this means chronic infectious diseases (e.g. chronic hepatitis) and acute infections with a core body temperature ≥ 38.0 °C) or unstable circulation (see exclusion criteria no. 7) within the last 3 months
- Uncontrolled high or low blood pressure defined as systolic blood pressure \>180 mmHg/\<100 mmHg and/or diastolic blood pressure \>115 mmHg (after three times measuring)
- Changes in lipid lowering medication within the last 2 weeks
- Intake of Angiotensin Converting Enzyme (ACE) inhibitor medication within a time interval of five times the terminal half-life of the ACE inhibitor before study start and during the study
- History of allergic reactions to anticoagulation
Key Trial Info
Start Date :
December 28 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 25 2021
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT03795038
Start Date
December 28 2018
End Date
May 25 2021
Last Update
July 28 2022
Active Locations (2)
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1
Nephrocare Rostock GmbH
Rostock, Mecklenburg-Vorpommern, Germany, 18059
2
Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden
Dresden, Saxony, Germany, 01307