Actively Recruiting
the Impact of Manual or Mechanical Ways to Perform PLR on the Accuracy of Evaluation of Fluid Responsiveness
Led by Southeast University, China · Updated on 2024-05-21
60
Participants Needed
1
Research Sites
112 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Our goal was to study the impact of different ways to perform passive leg raising (PLR) on the accuracy of evaluation of fluid responsiveness.
CONDITIONS
Official Title
the Impact of Manual or Mechanical Ways to Perform PLR on the Accuracy of Evaluation of Fluid Responsiveness
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with signs of tissue hypoperfusion such as rising lactate levels, need for vasopressors to maintain blood pressure, low urine output, or reduced consciousness who need fluid responsiveness evaluation
- Patients who have received Pulse indicator Continuous Cardiac Output (PiCCO) monitoring
- Patients transferred to the intensive care unit
You will not qualify if you...
- Age below 18 years or above 75 years
- Pregnancy or breastfeeding
- Refusal to sign informed consent
- Patients unable to perform passive leg raising due to high intra-abdominal pressure (≥16 cmH2O), high risk of lower limb venous thrombosis, intracranial hypertension, or recent abdominal or pelvic surgery
- Patients with contraindications to fluid resuscitation such as pulmonary edema or intracranial hypertension
- Patients assessed by doctors as unsuitable for passive leg raising
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Zhongda Hospital Southeast University
Nanjing, Jiangsu, China, 210009
Actively Recruiting
Research Team
J
Jingyuan Xu, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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