Magnetic Resonance Elastography of Transplanted Kidney (GREFFE_ELASTO IRM)

Interstitial Fibrosis/Tubular Atrophy of Transplanted Kidneys Clinical Trial

Official title:

Magnetic Resonance Elastography of Transplanted Kidney (GREFFE_ELASTO IRM)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03918161
• Other study ID #: CHUBX 2019/17
• Status: Completed
• Phase: N/A
• Start date: July 24, 2019
• Est. completion date: December 12, 2020

Study information

• Verified date: March 2021
• Source: University Hospital, Bordeaux
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

: GREFFE_ELASTO IRM will evaluate Magnetic Resonance Elastography (MRE) in renal transplant patients with suspected interstitial fibrosis/tubular atrophy lesions requiring biopsy graft sampling under ultrasound control. The main objective is to search a correlation between renal graft parenchymal elasticity values obtained in vivo by MRE, and the histological data of renal fibrosis by biopsy sampling, and providing a non-invasive tool capable of detecting and monitoring this development over time, making possible in the future to reduce the number of renal biopsies.

Description:

The natural history of interstitial fibrosis/tubular atrophy (IF/TA) is a common mechanism of disease progression of transplanted kidneys. The process has been well studied through protocol biopsies. The early phase is characterized by fibrogenesis and the emergence of tubulo-interstitial damage due to immunologic phenomena; the late phase is characterized by the worsening of parenchymal lesions and the occurrence of glomerular sclerosis leading to graft loss. Today, non-invasive markers of these pathological changes are missing and the protocol biopsies are still the only reliable tool for the diagnosis of IF/TA. Elasticity imaging has already been proven in the management of chronic liver diseases with Fibroscan. In the field of renal diseases, several studies have been carried out in ultrasound elastography on renal grafts but the renal elastography is more difficult due to the complexity of the kidney (deep organ, two compartments, high vascularity). All these parameters have an influence on the elasticity measures. The elastography imaging is also performed in MRI (Magnetic resonance imaging): The Magnetic Resonance Elastography (MRE). MRE is less subject to variations in depth, to the experience of the operator and to allow an overall evaluation of the graft. The potentially eligible patients will be recruited by the nephrologist during a consultation in which renal biopsy is scheduled (as part of current practice). Patients meeting the inclusion criteria and having no exclusion criteria will be offered to participate in this study. If accepted, the only examination specific to this research, the MRE, will be scheduled to be performed the same day as the renal biopsy. This MRE is painless, non-irradiating, and does not require the injection of contrast medium. The participation of the patient ends when he leaves the hospital after the biopsy procedure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 73
• Est. completion date: December 12, 2020
• Est. primary completion date: December 10, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Age = 18yrs;
• Transplanted kidney patient with suspicion of IF/TA lesions requiring biopsy graft sampling under ultrasound control;
• Signed informed consent;
• Affiliated or beneficiary of health insurance

Exclusion Criteria:

• Patients with dilated pyelocaliceal cavities on ultrasound or significant renal artery stenosis (> 80%) on Doppler;
• Pregnant or nursing women;
• Contraindications to MRI;
• Person deprived of liberty, major who is the subject of a legal protection measure or unable to express consent

Related Conditions & MeSH terms

• Atrophy
• Fibrosis
• Interstitial Fibrosis/Tubular Atrophy of Transplanted Kidneys

Intervention

Device:
• MRE exam
Magnetic Resonance Elastography

Locations

Country	Name	City	State
France	CHU Bordeaux	Bordeaux

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mean value of renal elasticity	5 times' measures in comparison with the upper pole of the graft which corresponds to the biopsy site (unit kilo-Pascal)	Baseline (defined as during MRE exam)
Secondary	Average value of renal elasticity	measured in 10 areas of the graft Intra-renal inflammation, tubulitis, chronic vascular and glomerular lesions measured semi-quantitatively by the pathologist following the Banff classification	Baseline (defined as during MRE exam)