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Clinical Trials/NCT05060614
NCT05060614
Recruiting
Not Applicable

MOLECULAR BIOMARKERS IN DELIRIUM AND DEMENTIA

Oslo University Hospital1 site in 1 country700 target enrollmentSeptember 1, 2016
ConditionsDelirium

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Delirium
Sponsor
Oslo University Hospital
Enrollment
700
Locations
1
Primary Endpoint
Delirium
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The current project aims to measure biomarkers in the cerebrospinalfluid (CSF) and serum samples from patients with delirium. We hope to uncover new insights into the pathophysiology of delirium and explore its link to dementia.

Detailed Description

Delirium is a common and serious complication to acute illness, and is characterized by acute disturbances in attention, awareness, and cognition. Dementia is a major risk factor of delirium, and delirium increases the risk of dementia progression and development. As the conditions share both clinical and epidemiological features, some researchers suggest that also pathophysiological links are shared. Understanding delirium pathophysiology, which is poorly understood, may thus help elucidate early molecular mechanisms in dementia. This study aims to to increase our understanding of the pathophysiology of delirium and molecular links between delirium and dementia, by exploring cerebrospinal fluid (CSF) biomarkers.

Registry
clinicaltrials.gov
Start Date
September 1, 2016
End Date
December 30, 2027
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Oslo University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Leiv Otto Watne

Postdoctoral Research Fellow

Oslo University Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with acute hip fracture

Exclusion Criteria

  • Moribund patients.
  • Lack of consent

Outcomes

Primary Outcomes

Delirium

Time Frame: Daily during hospital stay (pre-/and postoperatively) until 5 days after surgery (or discharge)

Pre- and postoperative delirium

Secondary Outcomes

  • Dementia(Cognitive changes the first 48 months after inclusion)

Study Sites (1)

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