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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03107455
Other study ID # EREMMI
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date December 1, 2021

Study information

Verified date March 2022
Source Fundación Investigación Sanitaria en León
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Acute MR may develop in the setting of an acute myocardial infarction (AMI) as a result of papillary muscle dysfunction or rupture, and these patients are grossly underrepresented in MitraClip registries. Our group has recently published the Spanish experience with MitraClip in acute MI, but only 5 patients could be collected. However, the results of our initial experience are highly encouraging since patients performed well in such life-threatening condition. In order to expand the information of the device in this condition, our aim is to start a multinational registry in Europe.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 1, 2021
Est. primary completion date July 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient = 18 year-old - Transmural myocardial infarction in the previous 4 weeks (managed under current guideline's recommendations). - Symptomatic severe mitral regurgitation diagnosed by left ventriculography, transthoracic echo or trans-oesophageal echo. Symptoms may vary form heart failure to cardiogenic shock. - Symptoms should be stabilized by medical management: iv diuretics, inotropic support, LV assistance devices - Considered by heart team at high risk for conventional surgery Exclusion Criteria: - Anatomy not suitable for MitraClip implantation - Technical contraindication for access to left atrium - Patient candidate for emergent heart transplant - Uncontrolled infection

Study Design


Intervention

Device:
MitraClip
MitraClip consists in two clip arms and opposing grippers, which can be opened and closed against each other in order to grasp and gain cooptation of MV leaflets at the origin of the regurgitant jet

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Fundación Investigación Sanitaria en León Abbott Medical Devices

Outcome

Type Measure Description Time frame Safety issue
Primary Composite primary end point death from cardiac causes, readmission due to heart failure and mitral regurgitation >2+ 6 month
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