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Clinical Trials/DRKS00007125
DRKS00007125Active, not recruiting未知

Modeling of lipoprotein in patients with familial hypercholesterolemia compared to healthy subjects

niversitätsklinikum Freiburg Institut für klinische Chemie und Laboratoriumsmedizin0 sites12 target enrollmentStarted: May 19, 2015Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Active, not recruiting
Sponsor
Enrollment
12

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Non-randomized controlled study
Masking
Open (masking not used)

Eligibility Criteria

Ages
18 Years to 75 Years (—)
Sex
Male

Inclusion Criteria

  • inclusion criteria for FH:
  • written consent
  • positive Simon Broome criteria (possible and definitely)
  • no lipid-lowering therapy in the 6 weeks before inclusion
  • inclusion criteria control subjects:
  • written consent
  • Patients without disorder of LDL metabolism, proven by< 200 mg/dl cholesteryl, < 150 mg/dl triglycerides and <160 mg/dl LDL-cholesteryl in fasting plasma
  • no relevant internistic deseases and no lipidlowering therapy in the 6 weeks before inclusion

Exclusion Criteria

  • 1.Active Liver-disease or impairment of liver function with GOT and/or GPT > 2 x value of the Upper Limit of Normal= (ULN)
  • 2.mid-level or severe renal insufficiency
  • 3.TSH not im reference range
  • 4.uncontrolled aterial hypertension: Diastolic RR = 105 mmHg and/or systolic RR = 160 mmHg
  • 5.lipid-lowering therapy within the last 6 weeks before the screening
  • 6.Smoker, alcohol abuse or other drug abuse
  • 7.blood donation within the last 6 weeks before the screening
  • 8.Patients with a adverse acute disease
  • 9. HbA1c > 6.5%
  • 10.Other important striking internistic diseases, which may alter the lipidmetabolism

Investigators

Sponsor
niversitätsklinikum Freiburg Institut für klinische Chemie und Laboratoriumsmedizin

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Modeling of lipoprotein in patients with... | Clinical Trial