- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05986812
SWE in Assessment of CKD Patients
August 3, 2023 updated by: Dina AbdAllah Noshy AbdAllah, Assiut University
Feasibility of Shear Wave Elastography in Assessment of Renal Stiffness in Chronic Kidney Diseased Patients
Elastography is a developing technique to assess tissue elasticity.
It is software that can be integrated to the ultrasonography machines.
Shear wave Elastography (SWE) is an Elastography technique that does not require external pressure on the tissue and supplies quantitative data.
It uses real-time short-duration acoustic push pulse to generate shear waves that propagate perpendicular to the main ultrasound beam.
When the waves hit the targeted tissue, the tissue is "pushed" in the direction of propagation, causing it to temporarily deform or displace.
The ultrasound scanner can monitor the tissue displacement, measuring the time-to-peak displacement and the recovery time.
Shear wave velocity increases in diseased tissues, which can be significantly stiffer than normal ones.
The parameters are expressed in pressure units of kilopascals (kPa) and velocity (m s-1).
SWE have been used to study breast, thyroid, prostate and liver diseases.
However, the application of SWE in assessment of renal fibrosis in CKD patients is still unclear.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
54
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
CKD patients which ages from 18 to 75 years old
Description
Inclusion Criteria:
- The patients are those older than 18 years diagnosed with CKD based on the KDIGO (Kidney Disease Improving Global Outcomes) definition i.e. eGFR less than 60 mL/min and/or the presence of markers of kidney damage (pathological albuminuria of at least 30 mg per 24 hours or proteinuria, hematuria, casts) persisting for more than 3 months.
Exclusion Criteria:
- Patients whose BMI >35kg/m 2 Any condition that precludes visualization of the kidney by ultrasound or transmission of shear waves as pregnancy or marked ascites patients with surgical kidney problems like hydro or pyonephrosis patients unwilling to complete the study. Patients with a history of renal replacement therapy (hemodialysis, peritoneal dialysis) , renal transplant, or acute kidney injury within the last 3 months Patients with cystic kidney disease Patients with renal masses
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Normal subjects
|
|
Diseased subjects
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The primary outcome of the study is the difference in renal SWE values between normal subjects and CKD patients .
Time Frame: From 2 to 3 years
|
From 2 to 3 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
October 25, 2023
Primary Completion (Estimated)
October 25, 2024
Study Completion (Estimated)
October 24, 2025
Study Registration Dates
First Submitted
July 25, 2023
First Submitted That Met QC Criteria
August 3, 2023
First Posted (Actual)
August 14, 2023
Study Record Updates
Last Update Posted (Actual)
August 14, 2023
Last Update Submitted That Met QC Criteria
August 3, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Renal Elastography
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Elastography ,CKD Patients
-
Sohag UniversityNot yet recruiting
-
Ain Shams UniversityMisr International University; October 6 UniversityCompletedCKD Anemia in Stable Dialysis Patients | CKD AnemiaEgypt
-
AstraZenecaActive, not recruitingRate of CKD Diagnosis in Patients With AH and CKD Markers | Demographic and Clinical Characteristics for Those Patients | Routine Therapy Before and After the Diagnosis of CKDKazakhstan
-
Sohag UniversityNot yet recruitingCKD on Hemodialysis Patients
-
National Taiwan University HospitalCompleted
-
Selcuk UniversityCompletedLiver Stiffness | Spleen Stiffness | Shear Wave Elastography in Healthy Children | Normal Organ Elasticity | Pediatric ElastographyTurkey (Türkiye)
-
Kastamonu UniversityNot yet recruitingElastography | Hallux Valgus Deformity
-
St George's, University of LondonCompletedCKd Patients With Stage 3 and 4
-
NYU Langone HealthWinthrop University HospitalCompleted
-
Assiut UniversityUnknownCKD Stage(III,IV,V) and Haemodialyzed Patients