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Functional and Clinical Impact of CYP3A Genetic Polymorphisms on Statin Therapy

Lipid-lowering Therapy Individualization

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01867203
Enrollment
0
Registered
2013-06-03
Start date
2017-08-01
Completion date
2019-09-01
Last updated
2021-03-18

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

Conditions

Patients With High Cholesterol Levels Needing a Lipid-lowering Therapy

Brief summary

Patients needing lipid lowering therapy will be recruited before initiation of the treatment. For each patient, total and LDL cholesterol levels before start of therapy will be measured. One, three and six months after his/her first visit, when steady-state will be reached, for each included patient, the cholesterol levels will be re-assessed in order to evaluate the response to statin therapy calculated as the amplitude of cholesterol reduction. The aim is to assess the association between patient's genotype and the response to statin therapy.

Interventions

OTHERGenotyping

DNA extraction from blood

Sponsors

Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
25 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patient known to be compliant * Age \[25-80\] * treated with Atorvastatin, simvastatin, fluvastatin.

Exclusion criteria

* Pregnancy

Design outcomes

Primary

MeasureTime frame
Cholesterol levels-side effects1 to 6 months

Countries

Belgium

Outcome results

None listed

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