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MRE Evaluation of Liver Stiffness After Tricuspid Valvular Repair

Evaluation of Liver Stiffness After Tricuspid Valvular Repair Using Magnetic Resonance Elastography

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03166488
Enrollment
0
Registered
2017-05-25
Start date
2017-05-01
Completion date
2018-12-31
Last updated
2018-06-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tricuspid Valve Insufficiency

Brief summary

The purpose of this study is to look at liver stiffness with a MRI sequence called Magnetic Resonance Elastography (MRE). The study will let the investigators know whether the subject's liver is normal or has increased stiffness. Increased liver stiffness often means there is chronic liver disease and fibrosis. Increased right heart pressure and congestive heart failure are considered risk factors for development of liver fibrosis. Liver fibrosis, if progressive, may lead to cirrhosis and its related complications. The increased liver stiffness may be due to a poorly functioning tricuspid valve. With this research, the investigators will be able to determine if the elevated stiffness of the liver returns to normal after the surgeon performs a repair or replacement of the tricuspid valve.

Interventions

DEVICEMRI

Subjects will receive an MRI sequence called Magnetic Resonance Elastography (MRE).

Sponsors

Mayo Clinic
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Primary tricuspid valvular regurgitation (tricuspid valve disease not related to a left-sided cardiac abnormality) diagnosed by echocardiography * Evidence of passive hepatic congestion. Patients with severe tricuspid regurgitation diagnosed at echocardiography will constitute evidence of passive hepatic congestion. * Patient scheduled for surgical tricuspid valvular repair or replacement.

Exclusion criteria

* Contraindication for MRI (implantable devices such as cardiac pacemaker, anxiety, inability to lay supine, etc). * Additional conditions which may elevate their liver stiffness: hepatic fibrosis or cirrhosis, hepatic parenchymal disease (primary biliary cirrhosis, primary sclerosing cholangitis, etc), acute or chronic hepatitis (viral, substance or medication induced), disorders of hepatic vasculature, biliary obstruction or disease, primary or metastatic hepatic malignancy. * Cannot agree to return for a follow up visit to complete the postsurgical imaging.

Design outcomes

Primary

MeasureTime frameDescription
Change in liver stiffness between preoperative and postoperative MR elastography (MRE)baseline, approximately 6 months postoperativelyIncreased liver stiffness often means there is chronic liver disease and fibrosis.
Change in tricuspid valve regurgitation measured by echocardiographybaseline, approximately 6 months postoperativelyIncreased liver stiffness may be due to a poorly functioning tricuspid valve.

Secondary

MeasureTime frameDescription
Change in Subject Functional Capacitybaseline, approximately 6 months postoperativelySubject Functional Capacity will be measured by the Self Assessment New York Heart Association (NYHA) Classification Scale. This questionnaire consists of 4 questions regarding the subject's ability to carry on physical activities. NYHA Class I = no symptoms in regular activity; NYHA Class II = Mild symptoms and slight limitation; NYHA Class III = noticeable limitations even during minimal activity; NYHA Class IV = severe limitations even while at rest.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026