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SuspendedNCT03953755STRONGUpdated Oct 20, 2022

Surgery in Secondary Tricuspid Regurgitation

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

Why this study was suspended
Slow recruitment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Jan 2019, registered May 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

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.

Read the detailed description

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:

  1. To study tricuspid regurgitation parameters affecting the long-term prognosis for the surgical correction of severe secondary tricuspid regurgitationof patients with severe aortic/mitral valve pathology requiring surgical treatment.
  2. To define hemodynamic parameters of patients with moderate tricuspid regurgitation, when surgical treatment of this defect gives an additional improvement in the short-term and long-term prognosis following surgical treatment of severe aortic/mitral valve diseases.
  3. To study changes in contractility parameters in the right ventricle and tricuspid valve function after reconstructive surgery over a period of 3 years.

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.

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Conditions studied

  • Tricuspid Regurgitation

Keywords

  • tricuspid regurgitation
  • tricuspid surgery
  • moderate tricispid
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In context

Tricuspid Valve Insufficiency

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 →

Lead sponsor

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.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Age > 18 years
  2. Indication left-side valve surgery

Exclusion criteria

Exclusion Criteria:

  1. Unwillingness to give informed consent and to enter a regular follow-up program.
  2. Prior surgical or percutaneous mitral valve intervention
  3. Contraindication to cardiopulmonary bypass (CPB)
  4. Clinical signs of cardiogenic shock at the time of randomization
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
150 participants (estimated)

Study arms

  • No intervention
    Control 1

    no/mild tricuspid regurgitation - left-side surgery alone

  • No intervention
    moderate TR - left-side surgery

    moderate tricuspid regurgitation - left-side surgery alone

  • Experimental
    moderate TR - left-side surgery+TVS

    moderate tricuspid regurgitation - left-side surgery+tricuspid valve surgery

    Procedure: Tricuspid valve repair

  • No intervention
    Control 2

    tricuspid regurgitation - left-side surgery +tricuspid valve surgery

Interventions

  • ProcedureTricuspid valve repair

    Tricuspid valve repair

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What researchers measure

Primary outcomes

  1. 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

  2. Difference in tricuspid annular plane systolic excursion

    Difference in TAPSE between of pre- and post- operation

    Time frame: 3 month, 1 year, 3 year

  3. 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

  4. 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

  5. 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

  6. tricuspid regurgitant volume

    tricuspid regurgitant volume

    Time frame: 3 month, 1 year, 3 year

  7. vtricuspid effective regurgitant oriface

    tricuspid effective regurgitant oriface

    Time frame: 3 month, 1 year, 3 year

  8. square of tricuspid regurgitation

    square of tricuspid regurgitation

    Time frame: 3 month, 1 year, 3 year

Secondary outcomes

  1. 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

  2. rate of all-cause death

    all-cause death

    Time frame: 3 month, 1 year, 3 year

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Study locations

1 site
  • St. Petersburg State University
    Saint Petersburg, 190103, Russian Federation
08

References and documents

Study documents

  • Informed consent form · Jun 6, 2018

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — Study protocol

Supporting information: Study protocol, Sap, Icf, Csr

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 20, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03953755
Lead sponsor
Saint Petersburg State University, Russia
Responsible party
Efremov Sergey (Deputy director for scince, Saint Petersburg State University, Russia) — Principal investigator
First posted
May 17, 2019
Start date
Jan 1, 2019
Primary completion
Dec 31, 2024 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Oct 20, 2022

Study contacts

Dmitry Shmatov, MD, PhD
principal investigator · Saint Petersburg State University, Russia

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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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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