Monitoring, Physiologic

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Review clinical trials related to Monitoring, Physiologic. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Paired Comparison of SVV and PVI Accuracy

This study will compare two operating-room monitors-stroke volume variation (SVV, from the arterial line) and the Pleth Variability Index (PVI, from the pulse oximeter)-to see which one more accurately predicts whether giving a small fluid bolus will improve the heart's pumping during laparoscopic major abdominal surgery. Adults having elective surgery under general anesthesia will receive two small, timed 250-mL crystalloid infusions as part of routine care (one before and one after creation of the pneumoperitoneum). The research team will record SVV and PVI values just before and three minutes after each infusion while keeping these readings hidden from the clinicians so that usual care is not changed. No experimental drugs or devices are used. The main goal is to learn which index better identifies "fluid responsiveness," so future care can be safer and more consistent. Potential risks are minimal and relate to the small fluid boluses (temporary changes in blood pressure or heart rate); the test stops if the anesthesiologist has any safety concerns. There is no direct benefit to participants, but results may help guide fluid therapy for similar patients in the future. The study is being conducted at a single academic hospital in the Republic of Korea and plans to enroll about 300 adults.

Participants needed: 300
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Wonkwang University HospitalUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Age ≥18 years [+5]

linically significant arrhythmia (e.g., atrial fibrillation with irregular R-R) [+6]

Status: Recruiting

Day Case Colectomy: Optimizing Short Stay-surgery.

HRV measurement of patients recovering from laparoscopic colorectal resection for any pathology.

Participants needed: 30
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: Joint Authority for Päijät-Häme Social and Health CareUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Non-Invasive Blood Pressure Monitoring in ICU Patients Using the DARE Device

This study tests a new non-invasive device called DARE to monitor blood pressure in patients in intensive care. It compares the device's readings to standard invasive methods and also looks at how well it measures other vital signs like temperature, oxygen levels, and heart rhythm. The goal is to improve patient safety and comfort while helping doctors detect problems earlier.

Participants needed: 2
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier de Saint-DenisUpdated: Jul 4, 2025Locations: 1
Eligibility criteria

Adult patients (male or female), aged 18 years or older [+3]

Patients under 18 years old (minors) [+8]