Ciclosporin to Protect Renal Function In Cardiac Surgery (CiPRICS)
Primary Purpose
Acute Kidney Injury
Status
Completed
Phase
Phase 2
Locations
Sweden
Study Type
Interventional
Intervention
Ciclosporin
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Acute Kidney Injury focused on measuring Ciclosporin, Acute Kidney injury, Cardiac surgery, Ischemia, Safety, Cystatin C
Eligibility Criteria
Inclusion Criteria:
- Non-emergent CABG
- Written informed consent to participate
- Preoperative CyC eGFR or MDRD eGFR is 90-15.
Exclusion Criteria:
- Uncontrolled hypertension
- Hypersensitivity to ciclosporin or any of the excipients of the lipid emulsion, including egg-, soya- or peanut protein
- Pregnancy or fertile woman
- Ciclosporin treatment within 4 weeks
- Ongoing malignancy, ongoing immunosuppressive treatment, severe hepatic dysfunction, dialysis or severe infection
- Ongoing medication with dabigatran, aliskiren, bosentan, stiripentol, glibenclamid, St John's worth, or
- Off-pump surgery
Sites / Locations
- Skane University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo
Ciclosporin
Arm Description
All components of the CicloMulsion® emulsion except ciclosporin: soybean oil (refined), triglycerides (medium-chain), egg lecithin, glycerol, oleic acid, sodium hydroxide and water for injection (=0.5 ml/kg).
Single dose of CicloMulsion® 5 mg/ml, 2.5 mg/kg (=0.5 ml/kg) as intravenous injection.
Outcomes
Primary Outcome Measures
Ciclosporin to Protect Renal function In Cardiac Surgery.
Relative P-CyC change from day -1 to day 3.
Secondary Outcome Measures
Full Information
NCT ID
NCT02397213
First Posted
March 12, 2015
Last Updated
October 12, 2016
Sponsor
Region Skane
Collaborators
NeuroVive Pharmaceutical AB
1. Study Identification
Unique Protocol Identification Number
NCT02397213
Brief Title
Ciclosporin to Protect Renal Function In Cardiac Surgery
Acronym
CiPRICS
Official Title
Ciclosporin to Protect Renal Function In Cardiac Surgery: CiPRICS A Phase II Double Blind Randomized Placebo Controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
April 2015 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
September 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Region Skane
Collaborators
NeuroVive Pharmaceutical AB
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate the potential of ciclosporin in reducing risk and degree of acute kidney injury after cardiac surgery.
Detailed Description
Acute kidney injury (AKI) is a common complication after cardiac surgery and is associated with decreased long-term survival. The mechanism for inducing acute kidney injury is unknown but ischaemia-reperfusion injury is indicated to be a part of the cause.
Animal studies have showed cytoprotective, preconditioning and anti-apoptotic effects of ciclosporin in ischaemia-reperfusion injury in the kidney. The major mechanism is thought to be inhibition of the reperfusion triggered opening of the mitochondrial permeability transition pore (mPTP), responsible for reperfusion-induced necrosis. During cardiac surgery, the period of extracorporeal circulation (ECC) changes the perfusion through the kidney. Return to normal perfusion with a beating heart has similarities with reperfusion following ischemia.
Administration of ciclosporin in conjunction with percutaneous coronary intervention (PCI), heart surgery and traumatic brain injury (TBI) in humans has shown to be safe with no direct side-effects.
The investigators therefore hypothesize that a preconditioning effect of ciclosporin before coronary artery bypass grafting (CABG) can reduce the level of renal dysfunction after this type of cardiac surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
Keywords
Ciclosporin, Acute Kidney injury, Cardiac surgery, Ischemia, Safety, Cystatin C
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
155 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
All components of the CicloMulsion® emulsion except ciclosporin: soybean oil (refined), triglycerides (medium-chain), egg lecithin, glycerol, oleic acid, sodium hydroxide and water for injection (=0.5 ml/kg).
Arm Title
Ciclosporin
Arm Type
Active Comparator
Arm Description
Single dose of CicloMulsion® 5 mg/ml, 2.5 mg/kg (=0.5 ml/kg) as intravenous injection.
Intervention Type
Drug
Intervention Name(s)
Ciclosporin
Other Intervention Name(s)
CicloMulsion® ATC-code: CO1EB
Intervention Description
Single dose of CicloMulsion® 5 mg/ml, 2.5 mg/kg (=0.5 ml/kg) as intravenous injection preoperatively after anesthesia induction.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
All components of the CicloMulsion® emulsion except ciclosporin: soybean oil (refined), triglycerides (medium-chain), egg lecithin, glycerol, oleic acid, sodium hydroxide and water for injection (=0.5 ml/kg).
Primary Outcome Measure Information:
Title
Ciclosporin to Protect Renal function In Cardiac Surgery.
Description
Relative P-CyC change from day -1 to day 3.
Time Frame
up to day 3
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Non-emergent CABG
Written informed consent to participate
Preoperative CyC eGFR or MDRD eGFR is 90-15.
Exclusion Criteria:
Uncontrolled hypertension
Hypersensitivity to ciclosporin or any of the excipients of the lipid emulsion, including egg-, soya- or peanut protein
Pregnancy or fertile woman
Ciclosporin treatment within 4 weeks
Ongoing malignancy, ongoing immunosuppressive treatment, severe hepatic dysfunction, dialysis or severe infection
Ongoing medication with dabigatran, aliskiren, bosentan, stiripentol, glibenclamid, St John's worth, or
Off-pump surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henrik Bjursten, Md, PhD
Organizational Affiliation
Skane University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Skane University Hospital
City
Lund
ZIP/Postal Code
22185
Country
Sweden
12. IPD Sharing Statement
Citations:
PubMed Identifier
27979834
Citation
Ederoth P, Grins E, Dardashti A, Bronden B, Metzsch C, Erdling A, Nozohoor S, Mokhtari A, Hansson MJ, Elmer E, Algotsson L, Jovinge S, Bjursten H. Ciclosporin to Protect Renal function In Cardiac Surgery (CiPRICS): a study protocol for a double-blind, randomised, placebo-controlled, proof-of-concept study. BMJ Open. 2016 Dec 15;6(12):e012299. doi: 10.1136/bmjopen-2016-012299.
Results Reference
derived
Learn more about this trial
Ciclosporin to Protect Renal Function In Cardiac Surgery
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