Fenoldopam for Prevention of Acute Kidney Injury (FANCY)
Primary Purpose
Coronary Artery Disease
Status
Unknown status
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
standard saline infusion
fenoldopam infusion
Sponsored by
About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring Contrast induced acute kidney injury
Eligibility Criteria
Inclusion Criteria:
- Indication to urgent/emergency coronary angiography
- Normal renal function (eGFR> 60 ml/min/1.73 m2)
- Moderate or high Mehran's risk score for CIN (>11).
- Able to understand and willing to sign the informed CF
Exclusion Criteria:
• Women of child bearing potential patients must demonstrate a negative pregnancy test performed within 24 hours before CT
Sites / Locations
- Sapienza University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
standard saline infusion
fenoldopam infusion
Arm Description
standard i.v. 1 ml/kg/h saline infusion from 6 hours before the procedure to 12 hours after the procedure.
combination of i.v. 1 ml/kg/h saline infusion and fenoldopam administration (0.08 mcg/Kg/min) from 6 hours before the procedure to 12 hours after the procedure.
Outcomes
Primary Outcome Measures
Contrast induced acute kidney injury
Incidence of contrast induced acute kidney injury at 48 hour post-procedural control
Secondary Outcome Measures
Markers of kidney injury
Post-angiographic 48-h absolute increase in creatinine, absolute increase in estimated glomerular filtration rate, and Neutrophil gelatinase-associated lipocalin (NGAL) value
Full Information
NCT ID
NCT01690832
First Posted
September 19, 2012
Last Updated
September 19, 2012
Sponsor
University of Roma La Sapienza
1. Study Identification
Unique Protocol Identification Number
NCT01690832
Brief Title
Fenoldopam for Prevention of Acute Kidney Injury
Acronym
FANCY
Official Title
Fenoldopam for Prevention of Acute kidNey Injury in Patients With aCute coronarY Syndrome Undergoing Coronary Angiography and/or Percutaneous Coronary Intervention - The FANCY Trial
Study Type
Interventional
2. Study Status
Record Verification Date
September 2012
Overall Recruitment Status
Unknown status
Study Start Date
September 2012 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
December 2014 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Roma La Sapienza
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Patients with acute coronary syndromes (ACS) are at increased risk for acute kidney injury (AKI) when they undergo urgent/emergency coronary angiography.
The optimal medical treatment for preventing the occurrence of contrast induced - acute kidney injury is still controversial.
Fenoldopam mesylate is a dopamine A1 receptor agonist that augments renal plasma flow that has reduced the risk of radiocontrast dye nephropathy in some (but not all) preliminary studies.
Neutrophil gelatinase-associated lipocalin (NGAL) is a new biomarker predictive for AKI already shown to be useful for earlier diagnosis of contrast induced nephropathy.
The primary objective of this study is to to test the hypothesis that fenoldopam, in addition to standard treatment, reduce the occurrence of contrast induced - acute kidney injury in patients with acute coronary syndrome (ACS) undergoing urgent/emergency coronary angiography and/or percutaneous coronary intervention.
Detailed Description
Patients with acute coronary syndromes (ACS) are at increased risk for acute kidney injury (AKI) when they undergo urgent/emergency coronary angiography.
The optimal medical treatment for preventing the occurrence of contrast induced - acute kidney injury is still controversial.
Fenoldopam mesylate is a dopamine A1 receptor agonist that augments renal plasma flow that has reduced the risk of radiocontrast dye nephropathy in some (but not all) preliminary studies.
Neutrophil gelatinase-associated lipocalin (NGAL) is a new biomarker predictive for AKI already shown to be useful for earlier diagnosis of contrast induced nephropathy.
The primary objective of this study is to to test the hypothesis that fenoldopam, in addition to standard treatment, reduce the occurrence of contrast induced - acute kidney injury in patients with acute coronary syndrome (ACS) undergoing urgent/emergency coronary angiography and/or percutaneous coronary intervention.
Patients will be randomized to standard i.v. 1 ml/kg/h saline infusion (Gr. A, N= 50) or to a combination of i.v. 1 ml/kg/h saline infusion and fenoldopam administration (0.08 mcg/Kg/min) from 6 hours before the procedure to 12 hours after the procedure.
Primary End-points
• Incidence of contrast induced acute kidney injury
Secondary End-points
• Post-angiographic 48-h absolute increase in creatinine, absolute increase in estimated glomerular filtration rate, and Neutrophil gelatinase-associated lipocalin (NGAL) value
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Contrast induced acute kidney injury
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
standard saline infusion
Arm Type
Active Comparator
Arm Description
standard i.v. 1 ml/kg/h saline infusion from 6 hours before the procedure to 12 hours after the procedure.
Arm Title
fenoldopam infusion
Arm Type
Active Comparator
Arm Description
combination of i.v. 1 ml/kg/h saline infusion and fenoldopam administration (0.08 mcg/Kg/min) from 6 hours before the procedure to 12 hours after the procedure.
Intervention Type
Drug
Intervention Name(s)
standard saline infusion
Other Intervention Name(s)
saline infusion
Intervention Description
i.v. 1 ml/kg/h saline infusion from 6 hours before the procedure to 12 hours after the procedure
Intervention Type
Drug
Intervention Name(s)
fenoldopam infusion
Other Intervention Name(s)
fenoldopam administration (0.08 mcg/Kg/min)
Intervention Description
combination of i.v. 1 ml/kg/h saline infusion and fenoldopam administration (0.08 mcg/Kg/min) from 6 hours before the procedure to 12 hours after the procedure
Primary Outcome Measure Information:
Title
Contrast induced acute kidney injury
Description
Incidence of contrast induced acute kidney injury at 48 hour post-procedural control
Time Frame
48 hour
Secondary Outcome Measure Information:
Title
Markers of kidney injury
Description
Post-angiographic 48-h absolute increase in creatinine, absolute increase in estimated glomerular filtration rate, and Neutrophil gelatinase-associated lipocalin (NGAL) value
Time Frame
48 hour
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Indication to urgent/emergency coronary angiography
Normal renal function (eGFR> 60 ml/min/1.73 m2)
Moderate or high Mehran's risk score for CIN (>11).
Able to understand and willing to sign the informed CF
Exclusion Criteria:
• Women of child bearing potential patients must demonstrate a negative pregnancy test performed within 24 hours before CT
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesco Pelliccia, MD
Organizational Affiliation
Sapienza University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sapienza University
City
Rome
State/Province
Lazio
ZIP/Postal Code
00166
Country
Italy
12. IPD Sharing Statement
Learn more about this trial
Fenoldopam for Prevention of Acute Kidney Injury
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