NCT Number: NCT02511418
Renal Hemodynamic Effects of the HMG-CoA Reductase Inhibitors in Normal Volunteers and in Patients With Chronic Renal Failure
This study was done to determine whether Simvastatin (a medication commonly used to treat patients with high cholesterol levels in the blood increases blood flow to the kidneys and improves renal function in normal volunteers and patients with impaired renal function secondary to polycystic kidney diseases.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Patients with chronic renal failure:
- Age 18 or older
- Chronic renal failure secondary to Autosomal Dominant Polycystic Kidney Disease
- Serum creatinine ≥ 1.4 but ≤ 2.0 mg/dl
- Creatinine or iothalamate clearance between 35-70 ml/min per 1.73m2
- Stable renal function for the three preceding months
- Blood pressure needs to be adequately controlled (< 140/90 mm Hg), with or without the use of antihypertensive agents. However, ACE inhibitors or AT1 receptor blockers must not be initiated, or have their dose increased during the study period.
Patients with normal renal function:
- Age 18 or older
- Normal renal function and diagnosed with Autosomal Dominant Polycystic Kidney Disease
- Serum creatinine ≤ 1.4
- Creatinine or iothalamate clearance ≥70 ml/min per 1.73m2
- Renal function has to be stable for the three preceding months
- Blood pressure needs to be adequately controlled (< 140/90 mm Hg), with or without the use of antihypertensive agents. However, ACE inhibitors or AT1 receptor blockers must not be initiated, or have their dose increased during the study period.
Exclusion criteria
include:
- Patients using corticosteroids, cytotoxic drugs (alkylating agents, chlorambucil, cyclophosphamide), CellCept, or cyclosporin A therapy
- Positive hepatitis B surface antigen (HBsAg) or hepatitis C antibody (HCV-Ab)
- Serum transaminase levels (AST, ALT) 2 times the upper limit of normal
- Clinically significant medical conditions
- Pregnant patients, patients who are breast-feeding, or women intending to conceive during the course of the study
- Presence or suspicion of active infection, recent serious infection or chronic/recurrent viral or bacterial infection
- Presence of concomitant renal artery stenosis.
Treatment and study plan
Primary outcomes
-
Effect of short term HMG-CoA reductase treatment
Time frame: 4 weeks
Differences between mean values for RPF, GFR and FF at baseline versus mean values obtained for these same parameters after 4 weeks of treatment will be analyzed using two-tailed Student's paired t-test. A similar analysis will be performed regarding patient's profiles for creatinine clearance, serum creatinine, urinary protein excretion and serum lipids. All results will be expressed as mean ± standard deviations. Differences will be considered significant at P <0.05.
Sponsors and collaborators
Lead sponsor
Mayo Clinic
Other
Registry information
Important dates
- Primary completion
- 2007
- First posted
- Jul 30, 2015
- Registry last updated
- Mar 16, 2023
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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