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Clinical Trials/NCT01384097
NCT01384097
Completed
N/A

An Algorithm for Intra-operative Goal-directed Haemodynamic Management in Non-cardiac Surgery - a Feasibility Study

Charite University, Berlin, Germany1 site in 1 country774 target enrollmentSeptember 2007

Overview

Phase
N/A
Intervention
Not specified
Conditions
Fracture of Surgical Neck of Humerus
Sponsor
Charite University, Berlin, Germany
Enrollment
774
Locations
1
Primary Endpoint
hospital length of stay
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

A systematic literature search a goal-directed haemodynamic algorithm was created. The hypothesis of this study was that the goal-directed haemodynamic algorithm is feasible and can improve clinical outcome.

Detailed Description

After a systematic literature search a goal-directed haemodynamic algorithm was created. The algorithm was adapted to international standards and consensus was reached through a modified Delphi method at international meetings. The feasibility of using the algorithm for intraoperative haemodynamic management was tested and the resultant clinical data analyzed retrospectively for several types of surgery with the hypothesis that the goal-directed haemodynamic algorithm is feasible in the clinical setting and can improve clinical outcome.

Registry
clinicaltrials.gov
Start Date
September 2007
End Date
June 2011
Last Updated
14 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Claudia Spies

Department of Anesthesiology and Intensive Care Medicine CVK/CCM, Charite University, Berlin

Charite University, Berlin, Germany

Eligibility Criteria

Inclusion Criteria

  • Patients undergoing a surgical repair of hip fractures, open right hemicolectomy and extended hemicolectomy, radical tumor debulking in primary ovarian cancer or a pylorus-preserving pancreatic head resection at the Charité - University Medicine Berlin, Campus Virchow Clinic
  • 18 years and older

Exclusion Criteria

  • emergency procedures

Outcomes

Primary Outcomes

hospital length of stay

Time Frame: a period of 60 days

The perioperative hospital length of stay is assessed.

Secondary Outcomes

  • need for ventilator therapy(a period of 60 days)
  • monetary reimbursement for prolonged hospital stay(a period of 60 days)

Study Sites (1)

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