跳至主要内容
临床试验/NCT07151989
NCT07151989Enrolling By Invitation不适用

Influence of Original Native Mitral Valve Lesion (Stenosis or Steno-insufficiency vs. Insufficiency) on Post-implant Structural Bioprosthetic Degeneration After Mitral Valve Replacement

Maastricht University Medical Center1 个研究点 分布在 1 个国家目标入组 3,500 人开始时间: 2024年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
3,500
试验地点
1
主要终点
Prosthesis degeneration due to physiological deterioration

研究概览

简要总结

It aims to perform a retrospective, multi-center, observational study. All patients undergoing elective mitral valve replacement from 2012 to 2021 who met the inclusion criteria for the study (described in the dedicated section) will be enrolled in the study. These patients will be followed-up as part of routine care, and information about the clinical status, NYHA functional class, possible rehospitalization, possible cardiovascular events and postoperative echocardiography will be available for analysis. Once consent is given, and if required by local governance, pre-, intra- and post-operative data will be collected in a dedicated, structured, database.

详细描述

It aims to perform a retrospective, multi-center, observational study. All patients undergoing elective mitral valve replacement from 2012 to 2021 who met the inclusion criteria for the study (described in the dedicated section) will be enrolled in the study. These patients will be followed-up as part of routine care, and information about the clinical status, NYHA functional class, possible rehospitalization, possible cardiovascular events and postoperative echocardiography will be available for analysis. Once consent is given, and if required by local governance, pre-, intra- and post-operative data will be collected in a dedicated, structured, database.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age ≥ 18 years;
  • •Patients who underwent isolated mitral valve replacement for stenosis or regurgitation
  • •Signed informed consent, inclusive of release of medical information where required by local governance.

排除标准

  • •- Aortic and mitral valve replacement associated with surgery of ascending aorta/aortic root;
  • •Aortic and mitral valve replacement associated with other cardiac valve surgery (apart from arrythmia-related ablation or procedures);
  • •Previous cardiac surgery of any kind;
  • •Surgery for acute endocarditis
  • •Surgery for Type A aortic dissection
  • •Participation in another clinical trial that could interfere with the endpoints of this study.
  • •Pregnant or breastfeeding at time of screening.

结局指标

主要结局

Prosthesis degeneration due to physiological deterioration

时间窗: 20 years

Echocardiographic paramters will be used. Quantitative and qualitative measurments swill be implied. The measurment used are listed below: 1. Morphological Assessment (2D / 3D TTE \& TEE) Leaflet morphology: thickness, mobility, calcification, pannus, tears, perforations. Bioprosthetic ring/annulus: dehiscence, rocking motion, paravalvular defects. Presence of thrombus, pannus, or vegetation. Structural valve deterioration (SVD) features: leaflet thickening, restricted opening, abnormal motion. 2. Hemodynamic Assessment (Doppler Echocardiography) Mitral inflow pattern (continuous-wave Doppler across prosthesis): Peak velocity (m/s) Mean transprosthetic gradient (mmHg) - heart-rate dependent Pressure half-time (PHT, ms) - limited use in prosthetic valves, but can suggest stenosis Effective orifice area (EOA) (via continuity equation or PHT-derived, cautiously interpreted). Doppler Velocity Index (DVI) = LVOT VTI / Prosthetic MV VTI (helps detect obstruction independent of fl

次要结局

  • Long term survival(20 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Roberto Lorusso

Prof. MD PhD

Maastricht University Medical Center

研究点 (1)

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