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Pleiotropism of Statin Therapy in High Dose Versus Low Dose Combined With Ezetimibe

Comparison of the Effect on Endothelial Function of Statin Therapy in High Dose Versus Low Dose Combined With Ezetimibe

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01241097
Enrollment
60
Registered
2010-11-16
Start date
2010-03-31
Completion date
2011-12-31
Last updated
2010-11-16

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

Conditions

Endothelial Function

Keywords

endothelial function, statins, ezetimibe, pleiotropism

Brief summary

* To test the hypothesis that therapy with high dose statin provides endothelial superior benefit to the same cholesterol lowering with low-dose statin combined with ezetimibe. * To test the hypothesis that therapy with high dose statin provides anti-inflammatory effect than the same reduction of cholesterol with low dose of statin plus ezetimibe

Detailed description

Randomized, double-blind, placebo-controlled study. Inclusion Criteria: Obese women with body mass index (BMI)\> 25 kg / m², aged 18 years and LDL-C\> 100 mg / dl For treatment with simvastatin 80 mg, the participant will receive two identical vials, each containing a simvastatin 40 mg. For treatment with the combination simvastatin 10 mg and ezetimibe 10 mg, the participant will receive two identical bottles, one bottle with simvastatin 10 mg, and another bottle with ezetimibe 10mg. In the control group, each participant will receive two identical bottles, each bottle containing inert tablets. Each group with 20 participants. Dependent Variable (Final Primary Outcome): Percentage change vasodilation of brachial artery flow-mediated, after treatment for eight weeks. Covariates: clinical, biochemical markers and ultrasound.

Interventions

DRUGsimvastatin, combined with simvastatin ezetimibe, placebo

simvastatin 80 mg per days or simvastatin 10 mg and ezetimibe 10 mg, over a period of eight weeks, treatment consisted of tablets identical, or placebo

Sponsors

Escola Bahiana de Medicina e Saude Publica
CollaboratorOTHER
Federal University of Bahia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Women with body mass index (BMI)\> 25 kg / m² * Aged \> 18 years * LDL-C\> 100 mg / dl

Exclusion criteria

* Previous use of statins, fibrates or ezetimibe * Triglycerides\> 400 mg / dl * Serum creatinine greater than 2.0 md / dl * Elevated liver enzymes, more than one and half times the upper limit of normal * Creatine kinase (CK) levels more than three times the upper limit of normal * Pregnant * Breast-feeding * Heart failure * Psychiatric disorders * Hormone replacement therapy. * The occurrence of recent onset within the last four weeks of treatment with beta-blockers, converting enzyme inhibitor or calcium channel blocker, the intervention should be undertaken after a period of at least four weeks of continuous use. * Acute inflammatory processes in the last month, assessed by clinical history and physical examination (ear, throat, skin lesions or other inflammatory manifestations) as well as reports of chronic diseases such as collagen, or the occurrence of active tuberculosis in the last three months will be excluded from work.

Design outcomes

Primary

MeasureTime frame
Percent change vasodilation of brachial artery flow-mediated, after eight weeks of treatment.8 weeks

Secondary

MeasureTime frame
biochemical markers8 weeks

Countries

Brazil

Contacts

Primary ContactMaristela M Garcia, MD
marismacardiol@gmail.com55-71-99739981
Backup ContactLuis Claudio L Correia, Phd
lccorreia@terra.com.br55-71-99711032

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026