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The effect of levosimendan on blood coagulation after cardiac surgery.

Conditions
Sepelvaltimotauti I20.0Sydämen vajaatoiminta I50.0
Registration Number
EUCTR2009-013957-13-FI
Lead Sponsor
Helsinki University Central Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
30
Inclusion Criteria

Vaseman kammion ejektio fraktio 30-50%
CABG leikkaus

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Munuaisten, maksan vajaatoiminta
Verenvuotosairaus
Antitromboottinen lääkitys mikäli ei ole keskitetty 7 päivää ennen leikkausta

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: Tutkimuksen tavoitteena on selvittää levosimendaanin vaikutusta veren hyytymiseen sydänleikkauksen jälkeen randomoidussa placebo-kontrolloidussa asetelmassa.;Secondary Objective: ;Primary end point(s): Tromboelastometria parametrit<br>Verihiutaleiden funktio (Multiplate)<br>Teho-hoitoaika
Secondary Outcome Measures
NameTimeMethod
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