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The Effect of Niacin Administration on Oxidative Stress in Patients With Hypercholesterolmia, as Measured by the Use of a Novel Biomarker

R

Rambam Health Care Campus

Status and phase

Unknown
Phase 3

Conditions

Hypercholesterolemia

Treatments

Drug: Niacin\Laropiprant

Study type

Interventional

Funder types

Other

Identifiers

NCT01071525
Niacin-OS

Details and patient eligibility

About

  1. Treatment of Hypercholesterolemic patients with niacin will cause a significant decrease in oxidative stress and a decrease in the atherogenecity in blood samples of the patients.
  2. A possible correlation between oxidative stress in hypercholesterolemic patients taking niacin to clinical hypercholesterolemia parameters is possible.
  3. Using a novel biomarker will enable a precise detection of the change in the oxidative stress in hypercholesterolemic patients.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Hypercholesterolemia,
  • age above eighteen

Exclusion criteria

  • Treatment with fibrates,
  • Pregnant/Breast feeding women

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Niacin
Active Comparator group
Description:
Hypercholesterolemic patients with high-density lipoprotein (HDL) less than 40 mg% will receive Niacin\\Laropiprant.
Treatment:
Drug: Niacin\Laropiprant
Control
No Intervention group
Description:
Maching subjects will receive no medication, Blood tests will be drawn for laboratory tests.
Treatment:
Drug: Niacin\Laropiprant

Trial contacts and locations

1

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Central trial contact

Shadi Hamoud, Dr

Data sourced from clinicaltrials.gov

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