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Kidney Disease and Ultrasound Imaging (Imag-NCT)

Primary Purpose

Recipient of Kidney Transplant

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
renal echography
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Recipient of Kidney Transplant focused on measuring Ultrasound functional imaging, Chronic kidney Nephropathy

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥ 18 years;
  • Patient with informed consent;
  • Recipient of a living donor graft or cadaveric donor patient;
  • No contraindication for biopsy of the graft;
  • No contraindication to the injection of SonoVue ®:

    • hypersensitivity to sulfur hexafluoride
    • acute coronary syndrome, unstable ischemic heart disease (myocardial infarction phase formation or evolution, typical resting angina in the previous 7 days, significant worsening of cardiac symptoms in the previous 7 days, recent intervention on the coronary arteries or another factor suggesting clinical instability (eg, recent deterioration of ECG changes in clinical or laboratory parameters), acute heart failure, stage III or IV heart failure, severe arrhythmias.
    • right-left shunt, severe pulmonary hypertension (PAP> 90 mmHg), uncontrolled systemic hypertension, respiratory distress syndrome
  • Affiliated to a social security scheme

Exclusion Criteria:

  • Refusal to participate in the study;
  • Inability / refusal to give informed consent;
  • contraindication for biopsy testing graft;
  • Presence of a contraindication to the injection of SonoVue ®.
  • Presence of a peripheral venous access in a non-restricted already infused patient, not pickable under ultrasound
  • Breastfeeding, pregnancy

Sites / Locations

  • NECKER Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Imag-NCT

Arm Description

The ultrasound functional imaging will be performed at J15 (before the patient is discharged from service Transplantation) and at 3 and 12 months after the transplant. The functional imaging examinations will be held as follows: 1st stage - the conventional Doppler ultrasound: 2nd stage - the elastography:. Step 3 - CEUS: It is performed on an ultrasound machine with a specific module with the same probes as conventional ultrasound. It requires the injection of 1.5 ml of SonoVue ®, a contrast ultrasound. Renal biopsy will be performed after the functional ultrasound at 3 and 12 months.

Outcomes

Primary Outcome Measures

renal Elastography
The assessment of renal function is performed by the serum creatinine and calculation of glomerular filtration rate estimated by the formula Modified Diet in Renal Disease (MDRD) 4-parameter at 3 and 12 months post-transplantation. In addition, a measure of glomerular filtration rate using the technique to iohexol is performed routinely at 12 months post-transplant as part of routine monitoring of transplant patient. The ultrasound functional imaging will be performed at 15 days, 3 and 12 months after transplantation. The functional imaging examinations will be held as follows: Step 1: the conventional Doppler ultrasound 2nd step: the ultrasound elastography Step 3 : CEUS
Renal Elastography and contrast-enhanced US
The assessment of renal function is performed by the serum creatinine and calculation of glomerular filtration rate estimated by the formula Modified Diet in Renal Disease (MDRD) 4-parameter at 3 and 12 months post-transplantation. In addition, a measure of glomerular filtration rate using the technique to iohexol is performed routinely at 12 months post-transplant as part of routine monitoring of transplant patient. The ultrasound functional imaging will be performed at 15 days, 3 and 12 months after transplantation. The functional imaging examinations will be held as follows: Step 1: the conventional Doppler ultrasound 2nd step: the ultrasound elastography Step 3 : CEUS

Secondary Outcome Measures

renal Elastography
Correlation between elastography and renal function with degree of fibrosis and renal function will be calculate using Pearson coefficient of correlation
Correlation between renal elastography and perfusion and degree of fibrosis and renal function
Correlation between elastography and renal function with degree of fibrosis and renal function will be calculate using Pearson coefficient of correlation
renal Elastography in patients with chronic kidney disease
this two measures will be express in evolution percentage at J15 and 3 months. The evolution percentage will be compared with imaging of patient with chronic kidney disease to determine if elastography and renal perfusion can predict chronic kidney disease at one year.

Full Information

First Posted
July 17, 2014
Last Updated
December 20, 2017
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fondation de l'Avenir, Bracco Imaging S.p.A.
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1. Study Identification

Unique Protocol Identification Number
NCT02201537
Brief Title
Kidney Disease and Ultrasound Imaging
Acronym
Imag-NCT
Official Title
Non-invasive Diagnosis of Chronic Kidney Disease in Renal Transplants Kidney Transplanted Using Ultrasound Functional Imaging
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
March 19, 2013 (Actual)
Primary Completion Date
March 19, 2016 (Actual)
Study Completion Date
March 19, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Fondation de l'Avenir, Bracco Imaging S.p.A.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The hypothesis of our study is that a correlation exists between the couple ultrasound elastography- renal perfusion estimated with contrast-enhanced ultrasound and the degree of fibrosis estimated in a semi-quantitative way in 4 stages (0; 25 %; 25-50 %; > 50 %), as elastography alone did not allow to differentiate moderated fibrosis at 3 months in our feasibility study.
Detailed Description
Kidney transplant patients are exposed to long-term immunosuppressive therapy, and have an increased risk of infections and cancer, while a lack of treatment increases the risk of rejection. The development of imaging techniques to characterize the status of the graft remains a challenge in transplantation. Ideally, they should identify complications (acute rejection, chronic allograft nephropathy, nephrotoxicity ...) without the need for invasive procedures and thus lead to better customization of immunosuppressive therapy. The post-transplant follow-up is based on the monitoring of graft function. Impaired function suggests the possibility of a complication, but requires confirmation by an invasive procedure such as renal biopsy. In addition, the diagnosis remains complex at a relatively advanced stage of the process due to damage to the graft parenchyma. To anticipate the altered function and detect subclinical lesions, screening biopsies have been used to diagnose chronic rejection. By definition, screening for subclinical lesions can not be based on any biological parameter; the diagnosis of subclinical complications thus requires performing multiple systematic biopsies, which are scheduled at 3 months and 1 year. Doppler ultrasound is an imaging method of choice for the study of renal transplant, but it cannot diagnose the NCT due to the absence of specific findings. The lack of early diagnostic test for NCT is a major obstacle to the development and evaluation of new therapeutic options to prevent, slow or stabilize renal fibrosis. It is therefore necessary to develop a non-invasive imaging technique for the early diagnosis of NCT. Ultrasound elastography is a technique that allows tissue stiffness measurements and provides a parametric picture. The main objective of our study is to evaluate the performances of elastography and measurement of renal perfusion (area under the ROC curve) to diagnose the NCT and determine for each both measures a threshold to maximize the sensitivity. These performances will be evaluated at 3 months and 12 months. The results can also be compared to other imaging modalities such as functional MRI, and to clinical events (obstruction, infection…). Functional ultrasound imaging should identify diagnostic and prognostic criteria of NCT, and enable the development of less invasive therapeutic protocols to evaluate new therapeutic approaches

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recipient of Kidney Transplant
Keywords
Ultrasound functional imaging, Chronic kidney Nephropathy

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
141 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Imag-NCT
Arm Type
Other
Arm Description
The ultrasound functional imaging will be performed at J15 (before the patient is discharged from service Transplantation) and at 3 and 12 months after the transplant. The functional imaging examinations will be held as follows: 1st stage - the conventional Doppler ultrasound: 2nd stage - the elastography:. Step 3 - CEUS: It is performed on an ultrasound machine with a specific module with the same probes as conventional ultrasound. It requires the injection of 1.5 ml of SonoVue ®, a contrast ultrasound. Renal biopsy will be performed after the functional ultrasound at 3 and 12 months.
Intervention Type
Device
Intervention Name(s)
renal echography
Intervention Description
Renal biopsy will be performed at 3 and 12 months. The functional imaging examinations will be held as follows: Step 1: the conventional Doppler ultrasound Step 2: ultrasound elastography Step 3: CEUS
Primary Outcome Measure Information:
Title
renal Elastography
Description
The assessment of renal function is performed by the serum creatinine and calculation of glomerular filtration rate estimated by the formula Modified Diet in Renal Disease (MDRD) 4-parameter at 3 and 12 months post-transplantation. In addition, a measure of glomerular filtration rate using the technique to iohexol is performed routinely at 12 months post-transplant as part of routine monitoring of transplant patient. The ultrasound functional imaging will be performed at 15 days, 3 and 12 months after transplantation. The functional imaging examinations will be held as follows: Step 1: the conventional Doppler ultrasound 2nd step: the ultrasound elastography Step 3 : CEUS
Time Frame
3 months
Title
Renal Elastography and contrast-enhanced US
Description
The assessment of renal function is performed by the serum creatinine and calculation of glomerular filtration rate estimated by the formula Modified Diet in Renal Disease (MDRD) 4-parameter at 3 and 12 months post-transplantation. In addition, a measure of glomerular filtration rate using the technique to iohexol is performed routinely at 12 months post-transplant as part of routine monitoring of transplant patient. The ultrasound functional imaging will be performed at 15 days, 3 and 12 months after transplantation. The functional imaging examinations will be held as follows: Step 1: the conventional Doppler ultrasound 2nd step: the ultrasound elastography Step 3 : CEUS
Time Frame
12 months
Secondary Outcome Measure Information:
Title
renal Elastography
Description
Correlation between elastography and renal function with degree of fibrosis and renal function will be calculate using Pearson coefficient of correlation
Time Frame
3 months
Title
Correlation between renal elastography and perfusion and degree of fibrosis and renal function
Description
Correlation between elastography and renal function with degree of fibrosis and renal function will be calculate using Pearson coefficient of correlation
Time Frame
12 months
Title
renal Elastography in patients with chronic kidney disease
Description
this two measures will be express in evolution percentage at J15 and 3 months. The evolution percentage will be compared with imaging of patient with chronic kidney disease to determine if elastography and renal perfusion can predict chronic kidney disease at one year.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years; Patient with informed consent; Recipient of a living donor graft or cadaveric donor patient; No contraindication for biopsy of the graft; No contraindication to the injection of SonoVue ®: hypersensitivity to sulfur hexafluoride acute coronary syndrome, unstable ischemic heart disease (myocardial infarction phase formation or evolution, typical resting angina in the previous 7 days, significant worsening of cardiac symptoms in the previous 7 days, recent intervention on the coronary arteries or another factor suggesting clinical instability (eg, recent deterioration of ECG changes in clinical or laboratory parameters), acute heart failure, stage III or IV heart failure, severe arrhythmias. right-left shunt, severe pulmonary hypertension (PAP> 90 mmHg), uncontrolled systemic hypertension, respiratory distress syndrome Affiliated to a social security scheme Exclusion Criteria: Refusal to participate in the study; Inability / refusal to give informed consent; contraindication for biopsy testing graft; Presence of a contraindication to the injection of SonoVue ®. Presence of a peripheral venous access in a non-restricted already infused patient, not pickable under ultrasound Breastfeeding, pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Michel CORREAS, PUPH
Organizational Affiliation
Necker Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
NECKER Hospital
City
Paris
ZIP/Postal Code
75015
Country
France

12. IPD Sharing Statement

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Kidney Disease and Ultrasound Imaging

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