Skip to main content
Clinical Trials/EUCTR2010-022816-38-SE
EUCTR2010-022816-38-SE
Active, Not Recruiting
N/A

Preoperative Optimization of the High-Risk Patient undergoing Hip Fracture Surgery - Hip-Op

Department of Anesthesiology & Intensive Care0 sites0 target enrollmentOctober 26, 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of Anesthesiology & Intensive Care
Status
Active, Not Recruiting
Last Updated
13 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 26, 2010
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Department of Anesthesiology & Intensive Care

Eligibility Criteria

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

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

Outcomes

Primary Outcomes

Not specified

Similar Trials