AzTrials
AzTrials

Acute Kidney DysfunctionPhase 2/3CREATNCT00910221

Cardiopulmonary-bypass and Reno-protective Effect of Atorvastatin Trial

A Phase 2/3 study testing Atorvastatin in people with Acute Kidney Dysfunction, run by Austin Health at 1 site in Australia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Acute kidney dysfunction is common after cardiac surgery. While many patients suffer no long-term ill effects from post-operative kidney dysfunction, some require initiation of dialysis therapy that can contribute to long-term morbidity. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Kidney Dysfunction
What is being tested?
Atorvastatin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
100 participants
Where
1 siteAustralia
Study dates
Mar 2008to Sep 2011
Phase
Phase 2/3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Cardiac surgical patients in whom the use of cardiopulmonary bypass was planned
  • Written informed consent of patient
  • Age > 18 years
  • And having at least one ore more of the following risk factors for postoperative AKI:
  • Age =/> 70 years
  • Preoperative plasma creatinine >120 µmol/L, New York Heart Association class III/IV or LVEF <35%
Show all 9Show fewer
  • Insulin dependent diabetes mellitus
  • Valve surgery (with or without coronary artery bypass graft)
  • Redo cardiac surgery

Who cannot join

  • An emergency operation is indicated (within 24 hours after hospital admission or on intra-aortic balloon pump)
  • Pregnancy is confirmed or breastfeeding is present
  • A renal allograft is present
  • Preoperative acute renal failure within 6 weeks (acute rise in serum creatinine > 50% from baseline) is present
  • Pre-operative end stage renal disease (serum creatinine > 300 µmol/L) is present
  • Chronic moderate to high dose corticosteroid therapy (>10 mg/d prednisone or equivalent) is present
  • Known Allergy to Atorvastatin

Trial locations and contacts

1 site in 1 country.

Australia1 site
  • Austin Health

    Melbourne, Victoria, 3084

Other trials in Australia

About this study

Official title: A Phase II Randomised, Double-blind, Placebo-controlled Study of the Effect of Atorvastatin on Postoperative Renal Function in Patients Undergoing Elective Cardiopulmonary Bypass.

Acute kidney dysfunction is common after cardiac surgery. While many patients suffer no long-term ill effects from post-operative kidney dysfunction, some require initiation of dialysis therapy that can contribute to long-term morbidity. Further, there is evidence to suggest that those patients requiring dialysis after cardiac surgery have a higher risk of death in hospital.

The exact reasons why some patients develop acute kidney dysfunction after cardiac surgery is not well understood. However, research evidence to date has suggested that the presence of co-morbid illnesses (i.e., diabetes mellitus) and exposure to cardiopulmonary bypass (heart-lung machine used during operation when heart is stopped). Cardiopulmonary bypass, in particular, has been shown to over-activate several aspect of the body's immune system. Such over-activity can induce oxidative stress and contribute to acute kidney dysfunction.

Read more

The investigators believe that the statin drug, atorvastatin, might reduce the oxidative stress that occurs during cardiopulmonary bypass, and thus, prevent or reduce the magnitude of acute kidney dysfunction in those patients at highest risk. The investigators hope to give atorvastatin (40 mg orally) to patients immediately prior to and for 3 days after cardiac surgery, and to compare the effects on kidney function with patients who have not had atorvastatin.

Atorvastatin is the most commonly prescribed medication in Australia and is used to reduce blood cholesterol levels and decrease the risk of heart attacks and stroke. Recently, however, it has been discovered that atorvastatin may be useful for prevention of inflammation and oxidative stress in other conditions, such as following cardiac surgery with cardiopulmonary bypass.

Thus, the investigators plan to examine whether atorvastatin can prevent acute kidney dysfunction. This trial as planned is a pilot study. If atorvastatin shows promising evidence of reduction in acute kidney dysfunction, further studies on a larger scale would be required to justify its general use.

The investigators plan to determine whether atorvastatin, a statin drug, possesses kidney protective effects in patients at risk for perioperative acute kidney dysfunction after cardiac surgery and exposure to cardiopulmonary bypass.

This is a pilot, randomized, blinded, placebo-controlled trial.

The investigators plan to administer atorvastatin (40 mg orally) or placebo to patients immediately prior to and for 3 days after cardiac surgery. The atorvastatin/placebo will be given orally either by orogastric tube after induction of anaesthesia or swallowed by the patients.

Whether a particular patient receives the atorvastatin or placebo will be decided at random, and neither the patient nor the investigators will be aware of the allocated treatment.

The investigators plan to measure kidney function before and after cardiac surgery using the standard blood tests. The investigators also plan to measure markers of inflammation and oxidative stress in the blood. This may give insight into the mechanisms whereby atorvastatin exerts its effects. The investigators will also take four 20 ml samples of blood, spaced before, and after the operation, from the arterial catheter routinely inserted in every patient undergoing cardiac surgery.

The investigators believe that there will be no significant additional risk to a patient who participates in the study, and no discomfort other than that normally associated with cardiac surgery. Informed consent will be obtained from the patient prior to the operation by one of the investigators or the ICU research nurse. The clinical care of a patient who does not consent for any reason will not be affected.

Being tested
Atorvastatin, Placebo
Keywords
Cardiac surgery, Cardiopulmonary bypass, Oxidative stress, Acute renal dysfunction, Atorvastatin

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AtorvastatinDrug

    Atorvastatin tablet

  • PlaceboDrug

    Placebo tablet

Study groups in NCT00910221
Study groupRoleWhat they receive
1Active comparatorNot described
Receives: Drug: Atorvastatin
2Placebo comparatorNot described
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in serum creatinine from baseline to peak level

    Measured: within first two-seven postoperative days

Secondary outcomes (8)
  1. Proportion of patients developing an increase in serum creatinine > 25% or >44µmicromol/L from baseline to peak level

    Measured: within first two-seven postoperative days

  2. Proportion of patients developing any of the RIFLE criteria: R, I or F

    Measured: within first seven postoperative days

  3. Proportion of patients developing any of the AKI stages: 1, 2 or 3 (using network definition)

    Measured: within first seven postoperative days

  4. Change in NGAL from baseline to peak

    Measured: within first 24 postoperatively

  5. Requirement of renal replacement therapy

    Measured: within hospital stay

  6. Length of stay in Intensive care

    Measured: from admission to discharge from Intensive care

  7. Length of stay in Hospital

    Measured: from admission to discharge from hospital

  8. Hospital-Mortality

    Measured: during hospital stay

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 May 2009 (estimated)
  2. Study startMar 2008
  3. Primary completionAug 2010
  4. Study completionSep 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00910221
Sponsor's protocol ID
H2007/02810
Acronym
CREAT
Status last verified
Aug 2009
First submitted
28 May 2009
Last updated
11 Sep 2012
Results posted
No
Data monitoring committee
Yes

Publications

  • Prowle JR, Calzavacca P, Licari E, Ligabo EV, Echeverri JE, Haase M, Haase-Fielitz A, Bagshaw SM, Devarajan P, Bellomo R. Pilot double-blind, randomized controlled trial of short-term atorvastatin for prevention of acute kidney injury after cardiac surgery. Nephrology (Carlton). 2012 Mar;17(3):215-24. doi: 10.1111/j.1440-1797.2011.01546.x.

    PubMed 22117606

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing Atorvastatin in people with Acute Kidney Dysfunction, run by Austin Health at 1 site in Australia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 9 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Sep 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in serum creatinine from baseline to peak level (time frame: within first two-seven postoperative days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00910221, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2012; AzTrials last refreshed its copy on 8 Nov 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in