Magnetic Resonance Imaging for Cerebral Embolization During Minimal Invasive Mitral Valve Surgery
Primary Purpose
Neurological Complications, Mitral Valve Insufficiency
Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Mitral valve surgery
Sponsored by
About this trial
This is an interventional treatment trial for Neurological Complications focused on measuring magnetic resonance, right mini-thoracotomy
Eligibility Criteria
Inclusion Criteria:
- Age between 18 and 80 years.
- Indication for elective mitral valve surgery +/- tricuspid valve surgery through right mini-thoracotomy.
- No contraindication for MR
Exclusion Criteria:
- Neuro-cognitive diseases;
- Peripheral vascular disease;
- Atrial fibrillation;
- PFO o interatrial defect;
- Previous Stroke;
- Autoimmune diseases;
- Neoplastic diseases;
- Migraine;
- Celiac disease;
- Alchool or drug abuse;
- Contraindication for MR.
Sites / Locations
- University of Turin - Cardiothoracic DepartmentRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Endoaortic Clamp
Transthoracic Clamp
Arm Description
Right mini-thoracotomy mitral valve surgery with retrograde perfusion and endoaortic balloon clamp
Right mini-thoracotomy mitral valve surgery with retrograde perfusion and transthoracic clamp.
Outcomes
Primary Outcome Measures
MR microembolization
To determine the incidence of new lesions on pre-discharge MR in patients undergoing right mini-thoracotomy mitral valve surgery according to different aortic clamping techniques.
Clinical events and MR outcome correlation
To assess the correlation between clinical neurological peri-procedural events (TIA, Stroke), cognitive / neuropsychological status and the occurrence of new lesions on pre-discharge MR.
Secondary Outcome Measures
Evolution of MR lesions
To assess the evolution of new cerebral ischemic lesions between pre-discharge MR and follow-up MR (3 months later)
Full Information
NCT ID
NCT02818166
First Posted
January 5, 2016
Last Updated
August 2, 2016
Sponsor
University of Turin, Italy
1. Study Identification
Unique Protocol Identification Number
NCT02818166
Brief Title
Magnetic Resonance Imaging for Cerebral Embolization During Minimal Invasive Mitral Valve Surgery
Official Title
Magnetic Resonance Neurological Evaluation After Right Mini-thoracotomy Mitral Valve Surgery: Trans-thoracic Versus Endoaortic Clamp
Study Type
Interventional
2. Study Status
Record Verification Date
August 2016
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
January 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Turin, Italy
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to prospectively evaluate major and minor neurologic events in patients undergoing right mini-thoracotomy mitral valve surgery and to compare different aortic clamping techniques; specifically, the endoaortic balloon with retrograde perfusion (Endoreturn) and the transthoracic clamp with retrograde perfusion. Major neurologic events will be evaluate through standard neurologic evaluation; minor neurologic events will be evaluate through magnetic resonance (MR) assessment.
The first aim of the study is to determine the number and impact of microembolic events during right mini-thoracotomy mitral valve surgery on clinical neurological status and on MR evaluation. The investigators also aim to determine if different techniques of aortic clamping may impact on early outcome.
Study hypothesis: despite recent concerns arising about endoaortic balloon with retrograde perfusion, the investigators expect to show equivalence in term of safety and effectiveness of this technique compared with the transthoracic clamp in a selected population.
Detailed Description
The incidence of neurologic events in right mini-thoracotomy mitral valve surgery compared with that of conventional surgery is a controversial issue and has been extensively studied. In the meta-analysis published by Modi et al, equal occurrence of neurologic events between patients who underwent MIMVS and those who underwent a median sternotomy was found. Conversely, the Thoracic Surgeons Adult Cardiac database and the Cleveland Clinic group concluded that the risk of stroke is significantly higher in the less invasive group.
Moreover, recent data have suggested that retrograde arterial perfusion, particularly in patients with severe arch/ascending aortic atherosclerosis, could be the source of the significant increase in the incidence of cerebral complications. The meta-analysis of Cheng, documents a 1.79 fold increase in the risk of stroke in the right thoracotomy group, but on subgroup analysis this appeared driven by a higher stroke risk in those studies reporting endoaortic balloon occlusion and not transthoracic clamping. Murzi et al. report a 4.28 fold increase in stroke risk with RAP in 1280 primary MIMVS patients. Grossi and colleagues show that the only significant risk factor for neurologic event was the use of retrograde perfusion in high-risk patients with aortic disease.
The purpose of this randomized blinded study is to prospectively evaluate major and minor neurologic events in patients undergoing right thoracotomy mitral valve surgery with retrograde perfusion and endoaortic balloon clamp (Endoreturn) or transthoracic clamp. Major neurologic events will be evaluate through standard neurologic evaluation; minor neurologic events will be evaluate through magnetic resonance assessment.
MR evaluation will be performed by blinded radiologists. MR will be performed with a 3T system (Philips INGENIA 3T). The protocol includes conventional sequences for the morphological and quantitative assessment (3D-FLAIR, 3D-T1-TSE, DWI, T2-FFE) and non conventional sequences for the white matter microstructural evaluation (Diffusion Tensor Imaging - DTI with fractional anisotropy and mean diffusivity). No contrast enhanced will be used.
Patients who have no contraindications will undergo cerebral MR before surgery as baseline assessment. Then, they will be randomized in one of the 2 groups.
If no contraindications arise in the postoperative period (eg definitive pacemaker implantation), patients will undergo cerebral MR before the discharge, to highlight the presence of new ischemic lesions, even clinically silent.
After 6 months, patients who developed new ischemic lesions revealed by the post-operative cerebral MR will repeat a new MR to assess evolution of cerebral damage Neurologic assessment will be performed by blinded specialists of the Neurology Department.
Type of the study:
Single center randomized blinded study that will be performed at the University of Turin, Città della Salute e della Scienza Hospital and will include:
Cardiac Surgery department. Neuroradiology department.
Aims of the study:
To determine the incidence of new lesions on pre-discharge MR in patients undergoing right mini-thoracotomy mitral valve surgery according to different aortic clamping techniques.
To assess the correlation between clinical neurological peri-procedural events (TIA, Stroke), and the occurrence of new lesions on pre-discharge MR.
To assess the evolution of new cerebral ischemic lesions between pre-discharge MR and follow-up MR (more than 6 months later).
To the investigators knowledge this is the first randomized blinded study that will compare two right mini-thoracotomy techniques for mitral valve surgery on a selected population (without risk factors for neurological events) with MR.
The result of this study will be able to allow surgeons to choose the best and less dangerous method in case of mini-invasive operations. This could rapresent a fundamental step in confirming the efficacy and safety of mini-invasive approaches for mitral valve surgery and resulting, in addition, in the reduction of the costs of these procedures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neurological Complications, Mitral Valve Insufficiency
Keywords
magnetic resonance, right mini-thoracotomy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care Provider
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Endoaortic Clamp
Arm Type
Experimental
Arm Description
Right mini-thoracotomy mitral valve surgery with retrograde perfusion and endoaortic balloon clamp
Arm Title
Transthoracic Clamp
Arm Type
Active Comparator
Arm Description
Right mini-thoracotomy mitral valve surgery with retrograde perfusion and transthoracic clamp.
Intervention Type
Procedure
Intervention Name(s)
Mitral valve surgery
Intervention Description
Right mini-thoracotomy mitral valve replacement/repair.
Primary Outcome Measure Information:
Title
MR microembolization
Description
To determine the incidence of new lesions on pre-discharge MR in patients undergoing right mini-thoracotomy mitral valve surgery according to different aortic clamping techniques.
Time Frame
untill 3 days after surgical procedure
Title
Clinical events and MR outcome correlation
Description
To assess the correlation between clinical neurological peri-procedural events (TIA, Stroke), cognitive / neuropsychological status and the occurrence of new lesions on pre-discharge MR.
Time Frame
untill 3 days after surgical procedure
Secondary Outcome Measure Information:
Title
Evolution of MR lesions
Description
To assess the evolution of new cerebral ischemic lesions between pre-discharge MR and follow-up MR (3 months later)
Time Frame
3 month follow up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age between 18 and 80 years.
Indication for elective mitral valve surgery +/- tricuspid valve surgery through right mini-thoracotomy.
No contraindication for MR
Exclusion Criteria:
Neuro-cognitive diseases;
Peripheral vascular disease;
Atrial fibrillation;
PFO o interatrial defect;
Previous Stroke;
Autoimmune diseases;
Neoplastic diseases;
Migraine;
Celiac disease;
Alchool or drug abuse;
Contraindication for MR.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cristina Barbero, MD
Phone
+390116335511
Email
cristina.barbero@unito.it
Facility Information:
Facility Name
University of Turin - Cardiothoracic Department
City
Turin
ZIP/Postal Code
10126
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mauro Rinaldi, MD
Phone
+390116335511
Email
mauro.rinaldi@unito.it
First Name & Middle Initial & Last Name & Degree
Cristina Barbero, MD
12. IPD Sharing Statement
Plan to Share IPD
Yes
Citations:
PubMed Identifier
28222779
Citation
Barbero C, Ricci D, Cura Stura E, Pellegrini A, Marchetto G, ElQarra S, Boffini M, Passera R, Valentini MC, Rinaldi M. Magnetic resonance imaging for cerebral lesions during minimal invasive mitral valve surgery: study protocol for a randomized controlled trial. Trials. 2017 Feb 21;18(1):76. doi: 10.1186/s13063-017-1821-y.
Results Reference
derived
Learn more about this trial
Magnetic Resonance Imaging for Cerebral Embolization During Minimal Invasive Mitral Valve Surgery
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