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OpenTrials
Completed

NCT Number: NCT00564434

Postoperative Delirium in Hip Fracture Patients

Risk factors for postoperative delirium in hip fracture patients.

Completed

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • hip fracture
  • age 65 or older

Exclusion criteria

  • critical ill/ dying
  • aphasia

Treatment and study plan

Primary outcomes

  1. Delirium/ no-delirium

    Time frame: 5 days postoperative

Secondary outcomes

  1. Severity of delirium, length of delirium, complications, comorbidity, one-year mortality.

    Time frame: 5 days postoperative, one year

Sponsors and collaborators

Lead sponsor

Ullevaal University Hospital

Other

Registry information

Important dates

Study start
2005
Study completion
2007
First posted
Nov 28, 2007
Registry last updated
Nov 28, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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