An interventional study of Tricuspid valve repair in Tricuspid Regurgitation, sponsored by Saint Petersburg State University, Russia. Suspended at 1 site in Russian Federation. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-10-20.
Sponsored by Saint Petersburg State University, Russia · Not applicable, Interventional, and Treatment
Currently, in cardiology/cardiosurgery the indicators for the surgical correction of secondary tricuspid regurgitationare unclear. AIM: To compare right ventricle structural and functional changes after operation in patients with secondary tricuspid regurgitation with severe mitral /aortic valve pathology, requiring surgical intervention; define the factors influencing major adverse cardiac events depending on the operation/non-operation due to moderate tricuspid regurgitation. This study intends to include 200-300 people and will occur over 5 years with an additional 3-year follow-up.
Background It has been demonstrated in recent large patient monitoring registers that the presence of even mild secondary tricuspid regurgitation (TR) has a significant effect on life expectancy. Currently, in cardiology/cardiosurgery the indicators for the surgical correction of secondary TR are unclear. In this area, international guidelines lack randomized studies and are based on a C level of evidence. C level evidence is based solely on the opinion of experts, retrospective, and/or observational studies. The first indicator for tricuspid valve (TV) surgery is considered to be a combination of TR with severe aortic or mitral valve lesions that require surgical treatment. However, the level of indicators for moderate corrections in such situations is typically II A-B. At the C level of evidence there is no consensus for surgical treatment of such a defect in the international community. Severe TR indicators are Class I while the evidence remains C level because it is not well established that surgical treatment improves the prognosis of these patients. There is a lack of information about the structural and functional changes of the right ventricle after surgery depending on the degree of TR.
Aims and objectives of studying AIM: To compare right ventricle structural and functional changes after operation in patients with secondary tricuspid regurgitation with severe mitral /aortic valve pathology, requiring surgical intervention; define the factors influencing major adverse cardiac events depending on the operation/non-operation due to moderate tricuspid regurgitation.
OBJECTIVES:
Methods and study plans This study intends to include 200-300 people and will occur over 5 years with an additional 3-year follow-up.
Inclusion criterion: 1) Signed informed consent form, 2) Previously diagnosed aortic or mitral heart diseases requiring surgical treatment, 3) Over 18 years of age 4) The presence of moderate or severe secondary tricuspid insufficiency.
Exclusion criterion: 1) Significant oncology diseases with a known prognosis of a less than 1 year life expectancy.
Cardiologist examination and survey. Echocardiography All patients will undergo standard echocardiography, including a detailed study of the function and sizes of the right ventricle and right atrium, and measurement of global longitudinal left ventricular deformations using the Speckle Tracking method, peak systolic and diastolic blood flow velocity in TV, fractional changes in area, and tricuspid annulus systolic excursion. Tricuspid regurgitation will be measured according to the standards of EAE/ASE, and will also use the recent 3-tiered classification system of severe insufficiency.
Laboratory techniques Standard for surgical treatment of aortic/mitral valve Coronary catheterization Standard for surgical treatment of aortic/mitral valve, Plan I. Initial visit - cardiologist/cardiosurgeon clinical evaluation - survey and examination II. Echocardiography study - screening - defining degree of tricuspid regurgitation III. Common tests for surgical treatment of aortic/mitral valve IV. Patient randomization with only a moderate degree of TR V. Surgical treatment VI. 30-40 days after surgery - cardiologist examination VII. 90 days after surgery ¬ - cardiologist examination + echocardiography VIII. 1 year after surgery - cardiologist examination + echocardiography IX. 3 years after surgery - cardiologist examination + echocardiography Expected benefits for patients All patients will receive advanced tests using the latest safe ultrasound methods. Frequent echocardiography and patient observations can reveal possible complications after cardiac surgery for aortic/mitral diseases; This study will allow for the correction of drug therapy due to extended diagnosis.
Severe lesions of the tricuspid valve and aortic / mitral heart defects will be corrected in all patients.
New and / or untested methods of treatment will not be used in this study. All surgical procedures will already have undergone testing and been proven effective for the treatment of heart diseases.
219 studies on the registry are indexed under Tricuspid Valve Insufficiency; 106 are open to participants now.
This study's planned enrollment of 150 is above the median of 60 across 118 interventional studies indexed under Tricuspid Valve Insufficiency.
Browse Tricuspid Valve Insufficiency studies →Saint Petersburg State University, Russia is the lead sponsor of 34 studies on the registry; 14 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
no/mild tricuspid regurgitation - left-side surgery alone
moderate tricuspid regurgitation - left-side surgery alone
moderate tricuspid regurgitation - left-side surgery+tricuspid valve surgery
Procedure: Tricuspid valve repair
tricuspid regurgitation - left-side surgery +tricuspid valve surgery
Tricuspid valve repair
Difference in end-diastolic dimension
Difference in end-diastolic dimension of right ventricle between of pre- and post- operation
Time frame: 3 month, 1 year, 3 year
Difference in tricuspid annular plane systolic excursion
Difference in TAPSE between of pre- and post- operation
Time frame: 3 month, 1 year, 3 year
Difference in right atrium volume index
Difference in right atrium volume index between of pre- and post- operation
Time frame: 3 month, 1 year, 3 year
Difference in fraction of area contraction of right ventricle
Difference in fraction of area contraction between pre- and post- operation
Time frame: 3 month, 1 year, 3 year
Difference in right ventricle global strain rate
Difference in right ventricle global strain rate between of pre- and post- operation
Time frame: 3 month, 1 year, 3 year
tricuspid regurgitant volume
tricuspid regurgitant volume
Time frame: 3 month, 1 year, 3 year
vtricuspid effective regurgitant oriface
tricuspid effective regurgitant oriface
Time frame: 3 month, 1 year, 3 year
square of tricuspid regurgitation
square of tricuspid regurgitation
Time frame: 3 month, 1 year, 3 year
major adverse cardiac events
death, myocardial infarction, new hospital readmission, heart transplant, ventricular assist device implantation, aborted sudden death, pulmonary oedema
Time frame: 3 month, 1 year, 3 year
rate of all-cause death
all-cause death
Time frame: 3 month, 1 year, 3 year
Documents are hosted by the registry — open the source record to download them.
Plan to share: Yes — Study protocol
Supporting information: Study protocol, Sap, Icf, Csr
This study is suspended, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.
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Tricuspid Valve Insufficiency→
Saint Petersburg State University, Russia