Actively Recruiting

All Genders
Healthy Volunteers
ID05060614

Molecular Biomarkers in Delirium and Dementia

Led by Oslo University Hospital · Updated on 2024-03-12

700

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating biomarkers in cerebrospinal fluid (CSF) and blood samples from patients experiencing delirium, a serious condition marked by sudden changes in attention, awareness, and thinking. The study aims to better understand how delirium relates to dementia, as both conditions share clinical features and may have linked biological causes. This research could reveal early molecular changes important for dementia development. Participants are patients with acute hip fractures who may undergo hip fracture surgery, which is observed in this study. The project collects CSF and serum samples to analyze biomarkers related to delirium and dementia. No experimental treatments are given, as this is an observational study focused on understanding disease mechanisms. During the hospital stay, delirium is monitored daily until five days post-surgery or discharge. Cognitive changes related to dementia are evaluated for up to 48 months after participation begins. The study involves collecting clinical data, samples, and cognitive assessments over time to explore how delirium may influence dementia progression. Participants' health and safety are observed throughout the follow-up period, which extends until the end date in 2027.

CONDITIONS

Brief Title

Analyses of Cerebrospinalfluid in Patients With Delirium

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with acute hip fracture
Not Eligible

You will not qualify if you...

  • Moribund patients
  • Lack of consent

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - Up to 5 days after surgery or until discharge

Participants undergo hip fracture surgery and are monitored daily for delirium during their hospital stay.

Daily visits during hospital stay

Long-term Monitoring

Duration - Up to 48 months

Participants are monitored for cognitive changes related to dementia for up to 48 months after inclusion.

Follow-up visits over 48 months

Trial Site Locations

Total: 1 location

1

Leiv Otto Watne

Oslo, Other, Norway, 0671

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Research Team

L

Leiv O Watne, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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