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Interest of Remote Ischemic Preconditioning for Prevention of Contrast Medium-induced Nephropathy in High Risk Patients (IPC-Angio)

Primary Purpose

Nephropathy

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Remote Ischemic Preconditioning (RIPC)
SHAM Remote Ischemic Preconditioning (SHAM RIPC)
Sponsored by
Rennes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Nephropathy focused on measuring Transcatheter Aortic Valve Implantation

Eligibility Criteria

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

Inclusion Criteria:

  • Age greater than 18 years, no upper age limit ;
  • Patient which may hospitalized for a medical check-up before a percutaneous aortic valve implantation (CTA and coronarography);
  • Patient at risk for NPCI defined by a Mehran risk classification system ≥11 (Annexe 2) ;
  • Willing to provide free and informed written consent

Exclusion Criteria:

  • Pathology of the upper-limbs limiting the use of the cuff (bilateral amputation, arteriovenous fistula);
  • Critical renal disease requiring hemodialysis ;
  • Person who is not affiliated to a health care system insurance
  • Inability to understand the instructions of the study;
  • Absolute contraindication to of iodinated contrast medium injection (anaphylactic shock history to contrast media, especially Xenetix, clearance (MDRD) less than 30mL/min/1.73m2) ;
  • Pregnancy
  • Simultaneous participation in other protocol;
  • Person with legal protection, person deprived of liberty.

Sites / Locations

  • Rennes University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Remote ischemic preconditioning

SHAM remote ischemic preconditioning

Arm Description

Remote Ischemic Preconditioning (RIPC) is accomplished by performing 4 cycles of alternating 5-minute inflation and 5-minute deflation of a standard upper-arm blood pressure cuff, to induce transient and repetitive arm ischemia and reperfusion. RIPC will be started just before the CTA, and the time between the last inflation cycle and the beginning of the CTA will be less than 45 minutes.

The SHAM Remote Ischemic Preconditioning ("SHAM" RIPC) will be carried out with the same number of cycles that the RIPC but cuff will be inflated to the diastolic pressure of the subject and the cuff will be deflated to10 mmHg in order to maintain a non- ischemic compression (blind patient protocol).

Outcomes

Primary Outcome Measures

Incidence of NPCI
Incidence of NPCI defined as an increase in serum creatinine ≥ 0.5 mg / dL or a relative increase of 25 % above baseline at 48 hours after contrast medium exposure.

Secondary Outcome Measures

Cystatin C
Changes of serum Cystatin C between day 0 and day 1, and day 0 and day 2.
Oxydative stress
Changes in markers of oxydative stress (in the first 40 patients included) : at day 0, after the RIPC procedure or SHAM-RIPC procedure (+ 5 min) before CTA ; after CTA (+ 30 min) and 24 hours after CTA (day 1).
Renal function
Changes in serum creatinine and Cystatin C between day 0 and measured values after coronarography (day 6 ).
Pain
A standardized pain scale (ranged from 0 to 10; 0 : no pain; 10 : maximum of pain).
Mortality
Assessment of mortality at six months.

Full Information

First Posted
June 5, 2015
Last Updated
May 22, 2023
Sponsor
Rennes University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02470247
Brief Title
Interest of Remote Ischemic Preconditioning for Prevention of Contrast Medium-induced Nephropathy in High Risk Patients
Acronym
IPC-Angio
Official Title
IPC-Angio Trial : Interest of Remote Ischemic Preconditioning for Prevention of Contrast Medium-induced Nephropathy (Post-diagnostic Imaging) in Patients at High Risk of Contrast-induced Nephropathy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
October 6, 2015 (Actual)
Primary Completion Date
August 24, 2017 (Actual)
Study Completion Date
October 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rennes University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Diagnostic imaging for vascular investigations and endovascular procedures frequently require the use of contrast medium. Besides contrast medium-induced hypersensitivity, an acute kidney injury can appear: the contrast-induced nephropathy (NPCI). NPCI is associated with an increase of patients' morbidity and mortality. One of the conventional methods proposed to limit this NPCI is an oral administration of N-acetylcysteine (NAC) associated with hydration performed 12 hours before and 12 hours after the injection. However, in some patients this method cannot be performed due to a high risk of heart failure although they are generally at high risk of NPCI. Recently, it has been shown, in a randomized trial, that remote ischemic preconditioning (several cycles of upper-arm ischemia-reperfusion with a pressure cuff inflator) associated with hydratation and NAC reduced the occurrence of NPCI after a coronary angiography as compared with NAC and hydration only. . We hypothesized that the use of RIPC in patients at high risk of NPCI and who cannot receive NAC and hydratation (e.g. patients with aortic stenosis and eligible for Transcatheter Aortic Valve Implantation (TAVI)) could be promising.
Detailed Description
Study design : Prospective, single-center, randomized, controlled, single-blind, with RIPC procedure (Pre-CI) versus "SHAM" ischemic preconditioning (SHAM Pre -CI) (control). This test will follow the CONSORT Statement (http://www.consort-statement.org/). This is a randomized, controlled, single-blind trial, assessing the incidence of NPCI (after a CTA ) between two group of patients, one receiving RIPC procedure and the other group receiving a "SHAM" RIPC (control group). RIPC is accomplished by performing 4 cycles of alternating 5-minute inflation and 5-minute deflation of a standard upper-arm blood pressure cuff, to induce transient and repetitive arm ischemia and reperfusion. RIPC will be started just before the CTA, and the time between the last inflation cycle and the beginning of the CTA will be less than 45 minutes. The "SHAM" RIPC will be carried out with the same number of cycles that the RIPC but cuff will be inflated to the diastolic pressure of the subject and the cuff will be deflated to10 mmHg in order to maintain a non- ischemic compression (blind patient protocol). Main objective : To assess the efficacy of remote ischemic preconditioning (RIPC) in preventing contrast-induced nephropathy (NPCI) after injected CT scanner in patients at high risk of NPCI. Secondary objectives : To assess the effects of RIPC on a second marker of renal failure (Cystatin C ) ; To determine the pathophysiological mechanisms involved in the RIPC (role of oxidative stress ; for the first 40 patients) ; To assess the effect of RIPC on renal function after a second injection of contrast-medium during coronary angiography performed 2 to 4 days after the injected CTA ; To assess the tolerance of RIPC procedure ; To assess the impact on mortality at 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephropathy
Keywords
Transcatheter Aortic Valve Implantation

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Remote ischemic preconditioning
Arm Type
Experimental
Arm Description
Remote Ischemic Preconditioning (RIPC) is accomplished by performing 4 cycles of alternating 5-minute inflation and 5-minute deflation of a standard upper-arm blood pressure cuff, to induce transient and repetitive arm ischemia and reperfusion. RIPC will be started just before the CTA, and the time between the last inflation cycle and the beginning of the CTA will be less than 45 minutes.
Arm Title
SHAM remote ischemic preconditioning
Arm Type
Sham Comparator
Arm Description
The SHAM Remote Ischemic Preconditioning ("SHAM" RIPC) will be carried out with the same number of cycles that the RIPC but cuff will be inflated to the diastolic pressure of the subject and the cuff will be deflated to10 mmHg in order to maintain a non- ischemic compression (blind patient protocol).
Intervention Type
Other
Intervention Name(s)
Remote Ischemic Preconditioning (RIPC)
Intervention Description
RIPC is accomplished by performing 4 cycles of alternating 5-minute inflation and 5-minute deflation of a standard upper-arm blood pressure cuff, to induce transient and repetitive arm ischemia and reperfusion. RIPC will be started just before the CTA, and the time between the last inflation cycle and the beginning of the CTA will be less than 45 minutes.
Intervention Type
Other
Intervention Name(s)
SHAM Remote Ischemic Preconditioning (SHAM RIPC)
Intervention Description
The SHAM Remote Ischemic Preconditioning ("SHAM" RIPC) will be carried out with the same number of cycles that the RIPC but cuff will be inflated to the diastolic pressure of the subject and the cuff will be deflated to10 mmHg in order to maintain a non- ischemic compression (blind patient protocol).
Primary Outcome Measure Information:
Title
Incidence of NPCI
Description
Incidence of NPCI defined as an increase in serum creatinine ≥ 0.5 mg / dL or a relative increase of 25 % above baseline at 48 hours after contrast medium exposure.
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Cystatin C
Description
Changes of serum Cystatin C between day 0 and day 1, and day 0 and day 2.
Time Frame
2 days
Title
Oxydative stress
Description
Changes in markers of oxydative stress (in the first 40 patients included) : at day 0, after the RIPC procedure or SHAM-RIPC procedure (+ 5 min) before CTA ; after CTA (+ 30 min) and 24 hours after CTA (day 1).
Time Frame
24 hours
Title
Renal function
Description
Changes in serum creatinine and Cystatin C between day 0 and measured values after coronarography (day 6 ).
Time Frame
6 days
Title
Pain
Description
A standardized pain scale (ranged from 0 to 10; 0 : no pain; 10 : maximum of pain).
Time Frame
Day 0
Title
Mortality
Description
Assessment of mortality at six months.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age greater than 18 years, no upper age limit ; Patient which may hospitalized for a medical check-up before a percutaneous aortic valve implantation (CTA and coronarography); Patient at risk for NPCI defined by a Mehran risk classification system ≥11 (Annexe 2) ; Willing to provide free and informed written consent Exclusion Criteria: Pathology of the upper-limbs limiting the use of the cuff (bilateral amputation, arteriovenous fistula); Critical renal disease requiring hemodialysis ; Person who is not affiliated to a health care system insurance Inability to understand the instructions of the study; Absolute contraindication to of iodinated contrast medium injection (anaphylactic shock history to contrast media, especially Xenetix, clearance (MDRD) less than 30mL/min/1.73m2) ; Pregnancy Simultaneous participation in other protocol; Person with legal protection, person deprived of liberty.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guillaume Mahe, MD
Organizational Affiliation
Rennes University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rennes University Hospital
City
Rennes
State/Province
Britanny
ZIP/Postal Code
35033
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
32729273
Citation
Belabbas D, Koch C, Chaudru S, Lederlin M, Laviolle B, Le Pabic E, Boulmier D, Heautot JF, Mahe G. Effects of Remote Ischemic Pre-Conditioning to Prevent Contrast-Induced Nephropathy after Intravenous Contrast Medium Injection: A Randomized Controlled Trial. Korean J Radiol. 2020 Nov;21(11):1230-1238. doi: 10.3348/kjr.2019.0916. Epub 2020 Jul 27.
Results Reference
result
PubMed Identifier
26802296
Citation
Koch C, Chaudru S, Lederlin M, Jaquinandi V, Kaladji A, Mahe G. Remote Ischemic Preconditioning and Contrast-Induced Nephropathy: A Systematic Review. Ann Vasc Surg. 2016 Apr;32:176-87. doi: 10.1016/j.avsg.2015.10.017. Epub 2016 Jan 21.
Results Reference
result

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Interest of Remote Ischemic Preconditioning for Prevention of Contrast Medium-induced Nephropathy in High Risk Patients

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