Elderly With Hip Fracture and Perioperative Hemoglobin and Perfusion Index Levels

NCT ID: NCT02838706

Last Updated: 2017-04-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-05-31

Study Completion Date

2016-12-01

Brief Summary

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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

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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.

Conditions

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Anemia Delirium

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Elderly with hip fracture

The subjects are patients age ≥ 65 years requiring surgery for a hip fracture

Surgery for hip fracture

Intervention Type PROCEDURE

Interventions

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Surgery for hip fracture

Intervention Type PROCEDURE

Eligibility Criteria

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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.
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hvidovre University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Christopher Clemmesen

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Copenhagen University Hospital Hvidovre, department of anesthesiology

Hvidovre, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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HvidovreUH

Identifier Type: -

Identifier Source: org_study_id

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