Ignite Creation Date:
2024-05-06 @ 4:09 PM
Last Modification Date:
2024-10-26 @ 2:05 PM
Study NCT ID:
NCT04899167
Status:
COMPLETED
Last Update Posted:
2023-10-05
First Post:
2021-05-19
Brief Title:
Noninvasive Evaluation of Renal Allograft Fibrosis by MRI
Sponsor:
Mayo Clinic
Organization:
Mayo Clinic
Study Overview
Official Title:
Noninvasive Evaluation of Renal Allograft Fibrosis by MRI
Status:
COMPLETED
Status Verified Date:
2023-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to validate an MRI method to detect renal fibrosis in patients after kidney transplantation KT
Detailed Description:
The hypothesis underlying this proposal is that qMT reliably detects development of allograft fibrosis in human subjects after KT To test this hypothesis the qMT-derived bound pool fraction will be correlated with renal fibrosis as per biopsy in 20 patients 4 or 7 years after living donor KT The bound pool fraction will also be compared to renal blood flow oxygenation and function and the ability of qMT to provide consistent assessments of fibrosis tested at different magnetic field strengths Two specific aims will test the hypotheses that Specific Aim 1 qMT provides reliable and consequential assessment of fibrosis in human kidney allografts Specific Aim 2 Renal fibrosis assessed by qMT in human kidney allografts is reproducible at 15 T and 30 T
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| R21AG062104 | NIH | None | httpsreporternihgovquickSearchR21AG062104 |