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Clinical Trials/NCT02838706
NCT02838706
Completed
Not Applicable

Contionuous Perioperative Hemoglobin and Perfusion Index Measurements in Elderly Patients With Hip Fracture and Post Operative Delirium

Hvidovre University Hospital1 site in 1 country50 target enrollmentMay 2016
ConditionsAnemiaDelirium

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Anemia
Sponsor
Hvidovre University Hospital
Enrollment
50
Locations
1
Primary Endpoint
Delay in diagnosting perioperative anemia
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The overall aim of the study is to investigate the time difference in the diagnosing of anemia among elderly with hip fracture, between measurements with standard blood samples and non-invasive SpHb-measuring. Another aim is to investigate the relationship between perfusion index and prolong perioperative anemia and the potential impact on perioperative complications.

Detailed Description

Immediately after admission and diagnosis of a hip fracture the patients will be monitored with Masimo SpHb. The Patients will be continuously measured until the third day after surgery. The Monitors Hb and PI data but not the SpO2% will be blinded to all participating healthcare personnel.The first three postopertive days the patiens will daily be examined to determined it they have developed delirium. All perioperativ complications in that period will be monitored.

Registry
clinicaltrials.gov
Start Date
May 2016
End Date
December 1, 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christopher Clemmesen

MD

Hvidovre University Hospital

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 65 years
  • Primary hip fracture requiring surgery
  • Patients able to give informed consent
  • Patients who are able to undergo the Hospitals standardized fast track
  • Perioperative care regimen for hip fracture including are pre operative placed epidural

Exclusion Criteria

  • Patients who can not co-operate to have a sensor attach to the finger continuous for 4 days.
  • Patients who has allergy to the bandage that is used to attach the sensor.

Outcomes

Primary Outcomes

Delay in diagnosting perioperative anemia

Time Frame: From admission up to and including the 3 postopertive day

Description of lag time between detection of anaemia by SpHb and Hb by blood sampling/transfusion

Perfusion index, periopertive anemia and delirium

Time Frame: From admission up to and including the 3 postopertive day

The relation between average perioperative perfusion index, cumulated perioperative anemia over time and patient outcome in the form of medical complications, mortality, delirium and LOS.

Secondary Outcomes

  • Perfusion index as a predictor of early warning score (EWS)(From admission up to and including the 3 postopertive day)

Study Sites (1)

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