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Atorvastatin treatment and vaccination efficacy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN87984926
Enrollment
312
Registered
2006-01-25
Start date
2004-11-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Hepatitis A Infections and Infestations Hepatitis A

Interventions

Subjects were immunised against hepatitis A and subsequently received atorvastatin (40 mg per day) or placebo for a period of 28 days after immunisation.

Sponsors

Geneva University Hospital (Switzerland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Men and women who were greater than 18 years old were eligible for inclusion if they had neither morbidities nor immunity to hepatitis A

Exclusion criteria

Exclusion criteria: 1. Anti-hepatitis A antibodies greater than 10 IU/l 2. Hypercholesterolemia 3. Hepatitis 4. Myositis 5. Chronic alcohol abuse 6. Pregnant or breast-feeding women 7. Volunteers on drug therapy except oral contraceptives

Design outcomes

Primary

MeasureTime frame
The main outcome variable was the achievement of antibody levels greater than 20 IU/l against the hepatitis A virus one month after vaccination.

Secondary

MeasureTime frame
1. A secondary outcome variable was the mean log-transformed antibody titre 2. To document the effects of atorvastatin on total blood cholesterol, Low Density Lipoprotein Cholesterol (LDL-C), High Density Lipoprotein Cholesterol (HDL-C), triglycerides, and high-sensitivity C-Reactive Protein (hs-CRP)

Countries

Switzerland

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026