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Pravastatin for Heart Disease
N/A
Waitlist Available
Research Sponsored by National Center for Research Resources (NCRR)
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
No history of hypertension
No history of coronary artery disease
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Study Summary
This trial will examine if pravastatin, an HMG-CoA reductase inhibitor, improves blood vessel functioning after a fatty meal.
Who is the study for?
This trial is for healthy individuals aged 18-40 without diabetes, high blood pressure, smoking habits, or heart disease. It's designed to see if pravastatin can prevent blood vessel issues after eating a fatty meal.Check my eligibility
What is being tested?
The study tests whether pravastatin improves how blood vessels function following a high-fat meal. Participants will be randomly given either pravastatin or a placebo for four days and then switch groups.See study design
What are the potential side effects?
Pravastatin may cause side effects like muscle pain, nausea, headache, and dizziness. However, it's generally considered safe with minimal side effects in most people.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have never been diagnosed with high blood pressure.
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I have never had heart artery disease.
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I have never been diagnosed with diabetes.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
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Who is running the clinical trial?
National Center for Research Resources (NCRR)Lead Sponsor
537 Previous Clinical Trials
317,016 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have never been diagnosed with high blood pressure.I have never had heart artery disease.I have never been diagnosed with diabetes.
Research Study Groups:
This trial has the following groups:Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is eligibility for this trial restricted to those younger than 65?
"Eligibility for this clinical trial stipulates that potential participants must be younger than 40 years old and at least 18."
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