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Preconditioning Against Renal Damage Under Contrast Examination (Re-DUCE-F)

Primary Purpose

Acute Kidney Injury

Status
Unknown status
Phase
Not Applicable
Locations
Ireland
Study Type
Interventional
Intervention
RIPC
Sponsored by
Mid Western Regional Hospital, Ireland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Kidney Injury focused on measuring Computerized Tomography, Contrast enhanced, Acute Kidney Injury, Remote ischaemic preconditioning, RIPC

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All medical and surgical in-patients aged 40-yrs or over scheduled to undergo contrast-enhanced CT scans.
  • Patients willing to give full informed consent for participation

Exclusion Criteria:

  • Pregnancy
  • Significant upper limb peripheral arterial disease
  • Previous history of upper limb deep vein thrombosis
  • Patients on glibenclamide or nicorandil (these medications may interfere with RIPC)
  • Patients with an estimated pre-operative glomerular filtration rate <30mls/min/1.73m2
  • Patients with a known history of myocarditis, pericarditis or amyloidosis
  • Patients who have received intravenous contrast in the previous year
  • Patients with severe hepatic disease defined as a an international normalised ratio >2 in the absence of systemic anticoagulation
  • Patients previously enrolled in the trial representing a further scan

Sites / Locations

  • University Hospital LimerickRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

RIPC

Control

Arm Description

Preconditioning will be performed in the same manner as several previous trials. Immediately prior to having the CT scan a CE-approved blood pressure cuff will be placed around one arm of the patient. It will then be inflated to a pressure of 200mmHg for 5 minutes. For patients with a systolic blood pressure >185mmHg, the cuff will be inflated to at least 15mmHg above the patient's systolic blood pressure. The cuff will then be deflated and the arm allowed reperfuse for 5 minutes. This will be repeated so that each patient receives a total of 4 ischaemia-reperfusion cycles.

Patients randomised to this group will receive routine care associated with undergoing a CT scan.

Outcomes

Primary Outcome Measures

Reduction in estimated glomerular filtration rate(eGFR) using RIPC
Our primary research objective is to determine whether RIPC induced using brief arm ischaemia and reperfusion reduces the proportion of patients who develop a reduction in estimated glomerular filtration rate(eGFR) ≥20% in the first 3 days following CT scan

Secondary Outcome Measures

Length of hospital stay
To determine whether RIPC reduces length of hospital stay
Length of intensive care stay
To determine whether RIPC reduces ITU stay
Numbers of unplanned critical care admissions
To determine whether RIPC reduces unplanned critical care admission
Renal impariment after 1 year
To determine the proportion of patients who develop renal impairment within 1 year of ce-CT
Recruitment potential for phase 3 study
To evaluate the likely recruitment rates for a phase 3 trial
Acceptability of intervention
To examine the acceptability of the intervention to clinicians and patients utilising qualitative methods
Cost effectiveness
To evaluate the cost-effectiveness of RIPC in the prevention of CI-AKI in patients undergoing ce-CT

Full Information

First Posted
February 3, 2014
Last Updated
February 3, 2014
Sponsor
Mid Western Regional Hospital, Ireland
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1. Study Identification

Unique Protocol Identification Number
NCT02054858
Brief Title
Preconditioning Against Renal Damage Under Contrast Examination
Acronym
Re-DUCE-F
Official Title
Preconditioning Against Renal Damage Under Contrast Examination: a Single Centre, Randomized, Sham -Controlled Clinical Feasibility Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Unknown status
Study Start Date
January 2014 (undefined)
Primary Completion Date
April 2015 (Anticipated)
Study Completion Date
June 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mid Western Regional Hospital, Ireland

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study aims to assess if applying an ischaemic insult to an arm before giving intravenous contrast will help decrease the incidence of developing contrast induced acute renal injury in patients undergoing contrast-enhanced CT Scans. The main research question is 'In adult in-patients undergoing contrast-enhanced CT scans, does remote ischaemic pre-conditioning (RIPC) induced by brief arm ischaemia and reperfusion, when compared to control, reduce the proportion of patients developing contrast-induced acute kidney injury in the first 3 post-scan days? '.
Detailed Description
Intravenous contrast for diagnostic and therapeutic interventions is a leading cause of hospital-acquired acute renal failure (1). Contrast-induced acute kidney injury (CI-AKI) occurs through a complex mechanism including toxic and hypoxic renal tubular injury, diminished renal parenchymal circulation and renal endothelial dysfunction with the production of oxygen free radicals due to post-ischaemia oxidative stress (2). With increasing numbers of diagnostic and therapeutic interventions, the incidence of CI-AKI will rise over the next few decades. Already, 40% of general surgical in-patients undergo cross-sectional imaging with computed tomography (CT), largely using contrast (3). Optimal clinical care in many specialties such as oncology, emergency medicine and surgery relies upon information derived from contrast-enhanced cross-sectional imaging. In consequence, large numbers of patients are exposed to the risk of CI-AKI. Current CI-AKI preventive measures comprise identification of at-risk patients, minimisation of contrast dose and the use of intravenous volume expansion (4). Simple, cost-effective methods to reduce CI-AKI are required. Risk factors for CI-AKI include advanced age, diabetes mellitus, pre-existing renal insufficiency and congestive cardiac failure. Dehydration also increases the risk (5). While patients over the age of 65 years currently account for 11% of the Irish population, they account for 30% of surgical admissions (6). In a recent cohort study of 1800 surgical in-patients in a major Irish teaching hospital, acute renal failure was a common major complication, occurring in 2.4% of patients (6). Multivariate analysis of this cohort demonstrated that increasing age and emergency admission were both independent risk factors for complications (6). Emergency surgical patients constitute a high-risk group in whom simple methods to minimise complications are required. Remote ischaemic preconditioning (RIPC) is a simple technique whereby brief periods of skeletal muscle ischaemia and reperfusion triggers a period of resistance to ischaemia-reperfusion injury in distant tissues e.g. heart or kidney (7). It reduces renal damage following endovascular aneurysm repair, a procedure requiring considerable contrast-volumes (8). A recent meta-analysis demonstrated that RIPC significantly reduced post-procedure creatinine levels following cardiovascular procedures, though there was considerable clinical heterogeneity between the included trials (9). We hypothesise that RIPC induced using brief periods of upper limb ischaemia-reperfusion will reduce AKI in patients undergoing contrast enhanced CT scans. The hypothesis that RIPC will reduce CI-AKI was first explored by Whittaker and Pryzklenk (10). They utilised available data from a patient cohort undergoing emergency coronary angioplasty. Patients with 1 to 3 balloon inflations in the coronary artery served as the control group whilst those with >3 balloon inflations served as the RIPC group.Both groups displayed an immediate improvement in estimated glomerular filtration rate (eGFR). However, the control group then displayed a statistically significant decrease in eGFR by day 3 post-procedure (77 +14 ml/min/1.73m2 versus 70 +12 ml/min/1.73m2). The RIPC group displayed no such difference by day 3 (81 +21 ml/min/1.73m2 versus 80 +14 ml/min/1.73m2) despite having received a larger contrast volume. This observation implied a potential protective effect for RIPC. Greater availability of CT technology has led to a dramatic increase in the number of patients undergoing ce-CTAP in recent years. Between 1996 and 2010, the number of patients undergoing CT scans in the United States tripled, increasing by 8% per annum (11). Simultaneously, an increasingly elderly and sick population means that many patients now have multiple co-morbidities, increasing their risk of contrast-induced acute kidney injury. Approximately 6.5% of patients undergoing ce-CT develop acute kidney injury defined as a >25% increase in serum creatinine from baseline (12). Simple methods to reduce CI-AKI are required. We propose that the use of remote ischaemic preconditioning could be a simple, cost-effective measure that could decrease the incidence of CI-AKI in high risk patients undergoing contrast enhanced CT scans.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
Keywords
Computerized Tomography, Contrast enhanced, Acute Kidney Injury, Remote ischaemic preconditioning, RIPC

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
1000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
RIPC
Arm Type
Experimental
Arm Description
Preconditioning will be performed in the same manner as several previous trials. Immediately prior to having the CT scan a CE-approved blood pressure cuff will be placed around one arm of the patient. It will then be inflated to a pressure of 200mmHg for 5 minutes. For patients with a systolic blood pressure >185mmHg, the cuff will be inflated to at least 15mmHg above the patient's systolic blood pressure. The cuff will then be deflated and the arm allowed reperfuse for 5 minutes. This will be repeated so that each patient receives a total of 4 ischaemia-reperfusion cycles.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients randomised to this group will receive routine care associated with undergoing a CT scan.
Intervention Type
Procedure
Intervention Name(s)
RIPC
Other Intervention Name(s)
Remote ischaemic preconditioning
Intervention Description
Remote ischaemic preconditioning (RIPC) is a simple technique whereby brief periods of skeletal muscle ischaemia and reperfusion triggers a period of resistance to ischaemia-reperfusion injury in distant tissues eg. heart or kidney. In this study preconditioning will be performed Immediately prior to the patient undergoing a CT scan. A CE-approved blood pressure cuff will be placed around one arm of the patient. It will then be inflated to a pressure of 200mmHg for 5 minutes. For patients with a systolic blood pressure >185mmHg, the cuff will be inflated to at least 15mmHg above the patient's systolic blood pressure. The cuff will then be deflated and the arm allowed reperfuse for 5 minutes. This will be repeated so that each patient receives a total of 4 ischaemia-reperfusion cycles.
Primary Outcome Measure Information:
Title
Reduction in estimated glomerular filtration rate(eGFR) using RIPC
Description
Our primary research objective is to determine whether RIPC induced using brief arm ischaemia and reperfusion reduces the proportion of patients who develop a reduction in estimated glomerular filtration rate(eGFR) ≥20% in the first 3 days following CT scan
Time Frame
3 days post scan
Secondary Outcome Measure Information:
Title
Length of hospital stay
Description
To determine whether RIPC reduces length of hospital stay
Time Frame
30 days
Title
Length of intensive care stay
Description
To determine whether RIPC reduces ITU stay
Time Frame
30 days
Title
Numbers of unplanned critical care admissions
Description
To determine whether RIPC reduces unplanned critical care admission
Time Frame
30 days
Title
Renal impariment after 1 year
Description
To determine the proportion of patients who develop renal impairment within 1 year of ce-CT
Time Frame
1 year
Title
Recruitment potential for phase 3 study
Description
To evaluate the likely recruitment rates for a phase 3 trial
Time Frame
15 months
Title
Acceptability of intervention
Description
To examine the acceptability of the intervention to clinicians and patients utilising qualitative methods
Time Frame
30 days
Title
Cost effectiveness
Description
To evaluate the cost-effectiveness of RIPC in the prevention of CI-AKI in patients undergoing ce-CT
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All medical and surgical in-patients aged 40-yrs or over scheduled to undergo contrast-enhanced CT scans. Patients willing to give full informed consent for participation Exclusion Criteria: Pregnancy Significant upper limb peripheral arterial disease Previous history of upper limb deep vein thrombosis Patients on glibenclamide or nicorandil (these medications may interfere with RIPC) Patients with an estimated pre-operative glomerular filtration rate <30mls/min/1.73m2 Patients with a known history of myocarditis, pericarditis or amyloidosis Patients who have received intravenous contrast in the previous year Patients with severe hepatic disease defined as a an international normalised ratio >2 in the absence of systemic anticoagulation Patients previously enrolled in the trial representing a further scan
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stewart R Walsh, MCh FRCS
Phone
00353 876632654
Email
stewart.walsh@ul.ie
First Name & Middle Initial & Last Name or Official Title & Degree
Mary Clarke Moloney, PhD
Phone
00353 61482736
Email
mary.clarkemoloney@hse.ie
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stewart R Walsh, MCh FRCS
Organizational Affiliation
University Hospital of Limerick
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Limerick
City
Limerick
ZIP/Postal Code
00
Country
Ireland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kamsila Pillay, MBChB, MRCS
Phone
003530877429483
Email
kamsilakp@yahoo.co.uk
First Name & Middle Initial & Last Name & Degree
Mary Clarke Moloney, PhD
Phone
00353 61482736
Email
mary.clarkemoloney@hse.ie
First Name & Middle Initial & Last Name & Degree
Stewart R Walsh, MCh FRCS
First Name & Middle Initial & Last Name & Degree
Kamsila Pillay, MBChB, MRCS
First Name & Middle Initial & Last Name & Degree
Mary Clarke Moloney, PhD
First Name & Middle Initial & Last Name & Degree
John Forbes, MSc PhD
First Name & Middle Initial & Last Name & Degree
Austin Stack, MD MSc FRCPI
First Name & Middle Initial & Last Name & Degree
Philip Hodnett
First Name & Middle Initial & Last Name & Degree
Tim Scanlon
First Name & Middle Initial & Last Name & Degree
Walter Cullen

12. IPD Sharing Statement

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Preconditioning Against Renal Damage Under Contrast Examination

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