Actively Recruiting
Cardiac Performance During Steep Trendelenburg Position in Patients Undergoing Robotic Surgery Surgery.
Led by Karlstad Central Hospital · Updated on 2026-02-12
80
Participants Needed
1
Research Sites
110 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The field of robotic-assisted laparoscopic surgery increases all the time. Older and more fragile patients which are not suitable for major open surgery could be scheduled for robotic- assisted surgery. The peroperative anesthesiological challenges and stresses during this type of surgery could anyway be even more prominent. The extreme positioning of patients during robotic surgery in the pelvis, often 30 degrees head down tilting (Trendelenburg positioning), should increase the work load of the heart significantly. There are no studies concerning fragile patients with heart failure during these conditions. In this study the circulatory effects in patients with normal heart function and preexisting heart failure will be studied during robotic surgery in extreme Trendelenburg positioning During surgery the work load and performance of the heart will be monitored using an esophageal doppler and optical spectrophotometry measuring regional saturation of the brain. This study can identify patients at risk of developing critical circulatory failure during this type of surgery.
CONDITIONS
Official Title
Cardiac Performance During Steep Trendelenburg Position in Patients Undergoing Robotic Surgery Surgery.
Who Can Participate
Eligibility Criteria
You may qualify if you...
1. Consecutive Patients Scheduled for Robotic Surgery with Trendelenburg positioning.
-
You will not qualify if you...
- Age <18;
- Dementia,
- Not able to give written consent -
AI-Screening
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Trial Site Locations
Total: 1 location
1
Dpt of Anesthesiology&Intensive Care; Central Hospital of Karlstad
Karlstad, Värmland County, Sweden, 65230
Actively Recruiting
Research Team
R
Ragnar N Henningsson, Associate Professor
CONTACT
A
Ann-Sofie Lorentzon, ND
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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