MRE Evaluation of Liver Stiffness After Tricuspid Valvular Repair

Sponsor
Mayo Clinic (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03166488
Collaborator
(none)
0
1
19

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: MRI
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Evaluation of Liver Stiffness After Tricuspid Valvular Repair Using Magnetic Resonance Elastography
Actual Study Start Date :
May 1, 2017
Anticipated Primary Completion Date :
Jun 1, 2018
Anticipated Study Completion Date :
Dec 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Tricuspid Valvular Repair Patients

Subjects will receive an MRI sequence called Magnetic Resonance Elastography (MRE) within 1 month preoperatively and as close to 6 months postoperatively as reasonably achievable.

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

Outcome Measures

Primary Outcome Measures

  1. Change in liver stiffness between preoperative and postoperative MR elastography (MRE) [baseline, approximately 6 months postoperatively]

    Increased liver stiffness often means there is chronic liver disease and fibrosis.

  2. Change in tricuspid valve regurgitation measured by echocardiography [baseline, approximately 6 months postoperatively]

    Increased liver stiffness may be due to a poorly functioning tricuspid valve.

Secondary Outcome Measures

  1. Change in Subject Functional Capacity [baseline, approximately 6 months postoperatively]

    Subject 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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts 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.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Michael L Wells, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michael L Wells, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT03166488
Other Study ID Numbers:
  • 16-009548
First Posted:
May 25, 2017
Last Update Posted:
Jun 13, 2018
Last Verified:
Jun 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 13, 2018