Not yet recruiting NCT07110506
Comparison of Hemodynamic Variables Between Using Conventional Invasive Catheter Monitoring and Non-invasive Piezoelectric Sensor
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Arterial pressure monitoring.
- Who it may be relevant to
- Registry conditions: Monitoring. Basic parameters: from 19 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Arterial pressure is obtained from invasive arterial monitoring and noninvasive arterial monitoring using piezoelectric sensor and compared.
Interventions
- Other Arterial pressure monitoring
Arterial pressure is monitored and obtained
Primary outcome measures
- Arterial pressure [Time frame: For 30 min after the induction of anesthesia,]
Eligibility criteria
Inclusion criteria
- Cases who require Invasive arterial pressure monitoring d/t bleeding.
Exclusion criteria
- Patients with cardiovascular disease, cerebrovascular diseases, renal disease, or Marfan syndrome
- Pregnancy
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Crossover
- Masking
- Triple blind
- Primary purpose
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07110506 · 202459