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OpenTrials
Completed

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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Key information

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

simvastatin

Drug

Primary outcomes

  1. 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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