About this trial
This study aims to evaluate the effectiveness of prewarming methods in preventing intraoperative hypothermia in patients undergoing HoLEP surgery. Designed as a randomized controlled study, patients who receive prewarming will be compared with those in the control group.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Male patients aged 18 years and older
Patients undergoing HoLEP surgery under general anesthesia
Patients who consent to participate in the study
Disqualifiers
Patients who refuse to participate in the study.
Patients unable to read, understand, or sign the informed consent form.
Hemodynamically unstable patients.
Patients with a preoperative or intraoperative body temperature >37°C.
Trial design
Parallel
Treatments tested in this trial
intraoperative body temperature
Diagnostic testBody temperature measurement with esophageal probe
Treatment groups
Trial outcomes
Primary outcomes
Time to onset of intraoperative hypothermia.
Time to develop intraoperative hypothermia (when body temperature drops below 36°C)
Secondary outcomes
Hemodynamic parameters
heart rate
Volume of irrigation fluid used
Volume of irrigation fluid used
Changes in body temperature
Changes in preoperative and intraoperative body temperature
Hemodynamic parameters
mean arterial pressure
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: