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PRECON 2 – Fast-track cardiac surgery (kvalitetssikringsprojekt).Remifentanyl anæstesi til koronar bypass (CABG) med eller uden samtidig udskiftning af aortaklappen (AVR) bedømt ved opvågningsforløb (ICU Discharge Score), kognitiv dysfunktion (tests), hæmodynamiske effekter (PAC/ekkokardiografi) og biokemiske markører (CKMB, TNT, pro-BNP, C-100).

Phase 1
Conditions
Anæstesi til hjertekirurgiske patienter.Studiet er randomiseret med inklusion af patienter til elektiv CABG med/ uden samtidig AVR med anvendelse af cardiopulmonal bypass. Patienter randomiseres til forskellig anæstesi regime.
MedDRA version: 12.1Level: HLTClassification code 10002092Term: Anaesthesia and allied procedures
MedDRA version: 12.1Level: LLTClassification code 10007530Term: Cardiac complications of anaesthesia or other sedation in labour and delivery
MedDRA version: 12.1Level: LLTClassification code 10012206Term: Delayed recovery from anaesthesia
MedDRA version: 12.1Level: LLTClassification code 10021722Term: Induction and maintenance anaesthesia
MedDRA version: 12.1Level: LLTClassification code 10031777Term: Other complications of anaesthesia or other sedation in labour and delivery
Registration Number
EUCTR2010-022428-58-DK
Lead Sponsor
Aarhus University Hospital, Skejby
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Patienter til elektiv CABG med/ uden samtidig AVR med anvendelse af cardiopulmonal bypass.
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

1. EF < 30%
2. Tidl. AMI indenfor 4 uger (i sig selv mulig prækonditionerende effekt)
3. Svær pulmonal hypertension (pMAP > 33% af MAP)
4. Arteriel hypertension (Sap > 180, Dap > 110)
5. NIDDM, IDDM, stoftskiftesygdomme
6. Antikoagulationsbehandling der kontraindicerer anlæggelse af epiduralkateter
7. Ikke brugbare ultralyds akustiske forhold.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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