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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03906734
Other study ID # 2017-01-12-3.1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 10, 2016
Est. completion date March 20, 2019

Study information

Verified date April 2019
Source Meshalkin Research Institute of Pathology of Circulation
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objective of the study: to evaluate whether alfieri technique improves clinical and hemodynamic results compared to transaortic mitral valve secondary cord cutting in patients scheduled to septal myectomy for severely symptomatic hypertrophic obstructive cardiomyopathy.


Description:

There is pilot prospective randomised study comparing immediate and early results of additional subvalvular mitral apparatus intervention versus additional alfieri stich in patients scheduled to septal myectomy for symptomatic obstructive cardiomyopathy.

Patients with proven hypertrophic cardiomyopathy and resting left ventricle outflow tract obstruction underwent septal myectomy. If patients were suitable for both surgical techniques, they were randomized to alfieri stich or secondary cord cutting. All surgeons were experienced at least 50 related procedures.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date March 20, 2019
Est. primary completion date October 28, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Hypertrophic obstructive cardiomyopathy

- Left ventricle outflow tract gradient > 50 mm Hg at rest

- Systolic anterior motion mediated mitral regurgitation

Exclusion Criteria:

- Intrinsic valvular heart disease

- Coronary artery disease

- Aortic disease

Study Design


Intervention

Procedure:
Septal myectomy
Transaortic septal myectomy
alfieri stich
Transaortic Mitral valve repair using alfieri technique
Subvalvular intervention
Transaortic Mitral valve subvalvular intervention including anterior mitral leaflet secondary cord cutting, papillary muscle release

Locations

Country Name City State
Russian Federation Novosibirsk State Research Institute of Circulation Pathology Novosibirsk

Sponsors (1)

Lead Sponsor Collaborator
Meshalkin Research Institute of Pathology of Circulation

Country where clinical trial is conducted

Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary Transmitral pressure gradient Transmitral pressure gradient after the procedures assessed by echocardiography 30-days
Secondary Repeat bypass Rate of second cross clamping and repeating bypass for procedure related reasons 30 day
Secondary Residual left ventricle outflow tract gradient Residual left ventricle outflow tract gradient assessed by direct measurement intraoperative measuerment
Secondary Early mortality All cause death during 30 days 30 days
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