Actively Recruiting
Perioperative Change in Blood Volume and Fluid Distribution in Total Hip Arthroplasty
Led by Copenhagen University Hospital, Hvidovre · Updated on 2025-03-21
25
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying changes in blood volume and fluid distribution around the time of surgery in patients undergoing total hip replacement. The study aims to better understand how blood volume changes during this surgery and how these changes relate to the occurrence of orthostatic intolerance, which is difficulty standing up without dizziness or fainting. This observational study uses a non-invasive carbon monoxide rebreathing method to measure blood volume accurately, as traditional assessments may not provide precise estimates. Participants will undergo carbon monoxide rebreathing measurements before surgery, and at 6 and 24 hours after surgery to track changes in total blood volume, hemoglobin, erythrocyte volume, plasma volume, and fluid distribution inside and outside cells. The study also measures inflammation markers like C-Reactive Protein and monitors orthostatic intolerance during mobilization after surgery. These measurements help describe how the body’s fluid and blood volumes shift during and after hip replacement surgery. During the study, participants will be assessed before surgery and at two postoperative times for blood volume and fluid changes, inflammation, and symptoms related to standing up. Researchers will analyze the association between blood loss and orthostatic intolerance, as well as inflammation and peripheral blood flow. The primary outcome is the change in total blood volume from before surgery to 6 hours after. Participants are involved only during the perioperative period, with all measurements conducted in the hospital setting.
CONDITIONS
Brief Title
Changes in Perioperative Blood Volume and Fluid Distribution in Patients Undergoing Primary Total Hip Replacement.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for an elective total hip arthroplasty in a standardized fast track setting
- Capable of participating in carbon monoxide rebreathing measurement
- Age 18 years or older
- Able to speak and understand Danish
- Has provided written informed consent
You will not qualify if you...
- Intraoperative blood loss exceeding 750 mL
- Perioperative need for a blood transfusion
- Confirmed or suspected coagulopathies
- Factors that make carbon monoxide rebreathing measurement impossible
- Known orthostatic intolerance
- American Society of Anesthesiologists physical status classification 4 or higher
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.
1 visit (in-person)
Duration - 1 day
Participants undergo measurements of blood volume and fluid distribution before surgery.
1 visit (in-person, preoperative)
Duration - 1 day
Participants undergo primary total hip replacement surgery with assessments of blood volume and fluid distribution up to 24 hours after surgery.
1 surgical visit and 2 post-operative visits within 24 hours
Duration - Up to 24 hours postoperatively
Participants are observed for changes in blood volume, fluid distribution, and related parameters up to 24 hours after surgery.
2 visits (6 hours and 24 hours postoperatively)
Trial Site Locations
Total: 1 location
1
Hvidovre University Hospital
Copenhagen, Denmark, 2960
Actively Recruiting
Research Team
P
Puk Kristiansen, MD
A
Ana-Marija Hristovska, Senior registrar, Ph.D.
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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