How Bleeding Affects Delirium in Older Patients With Hip Fractures: The IMPROVE-HIP Study
Condition(s) studied
Investigational drug(s) / intervention(s)
Blood Transfusion: Blood transfusion is given without delay (within 4 hours) in case of hemoglobin below our threshold.
Standard care: These patients recieve our standard care including blood transfusion as usual. Vital parameters and delirium screening are collected three times a day.
Study summary
The goal of this clinical trial is to investigate whether early detection of bleeding and prompt blood transfusions can help prevent delirium in patients aged 75 and older who are admitted to the hospital with hip fractures. The main question the trial aims to answer is:
Do patients aged 75 and older with hip fractures benefit from earlier treatment of anemia (low blood count) to reduce the risk of delirium?
Researchers will compare early diagnosis and treatment of bleeding with standard care to determine if it helps lower the risk of developing delirium.
Participants will:
Undergo blood tests, have their vital signs monitored, and be screened for delirium three times a day for the first 48 hours after surgery.
Receive blood transfusions promptly if their hemoglobin levels fall below a specified threshold.
Attend a follow-up visit at 30 days to assess cognitive function and overall quality of life.
Attend another follow-up at 90 days to evaluate hospital readmissions and survival.
Eligibility
Primary outcome measure(s)
- Number of Participants with Delirium — From enrollment to 48 hours after surgery
Occurence of delirium will be evaluted using screening methods three times a day.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Aarhus University Hospital | Aarhus | Central Jutland | Not Yet Recruiting |
| Gødstrup Hospital, Department of internal medicine | Herning | Central Jutland | Recruiting |
More University of Aarhus trials in Denmark
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06938789 on ClinicalTrials.gov ↗ ← All trials in Denmark