Data analysis on the use of synthetic tendinous cords for mitral valve reconstruction

Data analysis on the use of synthetic tendinous cords for mitral valve reconstruction - VS-MKR

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00028272

Enrollment

100

Registered

2023-01-18

Start date

2023-03-27

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I34.0

Interventions

Group 1: All patients admitted to the Heart Centre for planned mitral valve reconstruction are asked whether they would like to take part in the project

information and consent are given on the basis of the patient information and consent form. The mitral valve reconstruction is performed using SERAMON® Chordae Loops from Serag Wiessner. In addition t

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients in whom a primary mitral valve reconstruction is planned (isolated MKR or combined MI/TI surgery); presence of the written consent form.

Exclusion criteria

Exclusion criteria: Emergency surgery; Presence of endocarditis

Design outcomes

Primary

Measure	Time frame
Mitral valve regurgitation after surgery, at discharge, at follow ups	—

Secondary

Measure	Time frame
Re-operation, death of the patient, endocarditis, embolisation (stroke)	—

Countries

Germany

Contacts

Public ContactHeike Windhagen

Herz- und Diabeteszentrum NRW, Klinik für Thorax- u. Kardiovaskularchirurgie, Universitätsklinikum der Ruhr Universität Bochum

hwindhagen@hdz-nrw.de05731-97-1907

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026