Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Patients with acute hip fracture
You will not qualify if you...
- Moribund patients
- Lack of consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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
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
Actively Recruiting
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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