Aprotiinin keuhkojen toimintaa suojaava vaikutus sydänleikkauksissa

• Conditions: ohitusleikkaus; MedDRA version: 8.1Level: LLTClassification code 10011098Term: Coronary bypass

• Registration Number: EUCTR2006-004866-14-FI
• Lead Sponsor: TAYS

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2006-09-04
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

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

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main Objective: aprotiinin vaikutus keuhkojen suojaamisen sydänleikkauksen aikana;Secondary Objective: ;Primary end point(s):