EUCTR2010-022816-38-SEActive, not recruitingNot Applicable
Preoperative Optimization of the High-Risk Patient undergoing Hip Fracture Surgery - Hip-Op
Department of Anesthesiology & Intensive Care0 sites0 target enrollmentStarted: October 26, 2010Last updated:
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •Inclusions Criteria:
- •1.Patients >= 65 yrs
- •2.Proximal femur fracture where the patient is planned to be operated during the day (Monday-Friday).
- •3.NT-proBNP > 900 ng/l in patients 65-75 yrs old, and >1800 ng/l in patients > 75 yrs.
- •4.Informed consent provided by the patient.
- •All of the above criteria must be fulfilled before the patient can be included in the study.
- •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
- •Exclusions Criteria:
- •1.Informed consent cannot be provided
- •2.Mental or verbal difficulty in understanding or expressing willingness to participate in the study.
- •3.Instable angina pectoris.
- •4.Ongoing myocardial infarct or ischemia
- •5.Circulatory shock
- •6.Decompensated cardiac failure or pulmonary oedema
- •7.Pathologic femur fracture
- •8.Chronic haemodialysis
- •9.Cardiac valve incompetence that has haemodynamic consequences
- •Any one of the above is a criterion for exclusion.
Investigators
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