Ignite Creation Date:
2025-12-25 @ 12:07 AM
Ignite Modification Date:
2025-12-25 @ 10:06 PM
Study NCT ID:
NCT04423458
Status:
COMPLETED
Last Update Posted:
2023-02-08
First Post:
2020-06-05
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Evaluation of Advanced US Tools in Assessing Allograft Complications
Sponsor:
Imperial College London
Organization:
Study Overview
Official Title:
The Evaluation of Advanced Ultrasonography Applications in the Assessment of Transplanted Kidney Complications
Status:
COMPLETED
Status Verified Date:
2023-02
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:
This study evaluates the role of advanced US technology in assessing renal transplants as screening tools such as 3D Ultrasound, Ultrasound SWE, and MFI besides current ultrasound conventional metheds.
Detailed Description:
This study will focus on monitoring renal after transplantation using all US advanced technology.
Aim one will concentrate on the 3D US in assessing artery stenosis (TRAS) compared to the gold standard.
Aim two focuses on will concentrate on Ultrasound elastography in assessing renal stiffness.
Aim three will compare US colour modes such as PD, CD and MFI to assess renal perfusion in three groups.
Duration: 18 Months; participants will have a patient information sheet; once they are happy to participate, consent will be obtained.
Study data will be entered into a database encrypted and stored in the department. Only the study principal investigator (PI) will know the study database password.
Aim one will concentrate on the 3D US in assessing artery stenosis (TRAS) compared to the gold standard.
Aim two focuses on will concentrate on Ultrasound elastography in assessing renal stiffness.
Aim three will compare US colour modes such as PD, CD and MFI to assess renal perfusion in three groups.
Duration: 18 Months; participants will have a patient information sheet; once they are happy to participate, consent will be obtained.
Study data will be entered into a database encrypted and stored in the department. Only the study principal investigator (PI) will know the study database password.
Study Oversight
Has Oversight DMC:
False
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?: