Postoperative Delirium in Hip Fracture Patients

November 27, 2007 updated by: Ullevaal University Hospital
Risk factors for postoperative delirium in hip fracture patients.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment

364

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Norway
      • Oslo, Norway
        • Ullevaal Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Study Population

Patients with hip fracture admitted to Ulleval Hospital and Diakonhjemmet Hospital

Description

Inclusion Criteria:

  • hip fracture
  • age 65 or older

Exclusion Criteria:

  • critical ill/ dying
  • aphasia

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Delirium/ no-delirium
Time Frame: 5 days postoperative
5 days postoperative

Secondary Outcome Measures

Outcome Measure
Time Frame
Severity of delirium, length of delirium, complications, comorbidity, one-year mortality.
Time Frame: 5 days postoperative, one year
5 days postoperative, one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Ullevaal University Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

May 1, 2005

Study Completion (Actual)

January 1, 2007

Study Registration Dates

First Submitted

November 27, 2007

First Submitted That Met QC Criteria

November 27, 2007

First Posted (Estimate)

November 28, 2007

Study Record Updates

Last Update Posted (Estimate)

November 28, 2007

Last Update Submitted That Met QC Criteria

November 27, 2007

Last Verified

November 1, 2007

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 1.2005.812

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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