Comparison of the Effect of Prewarming on Intraoperative Hypothermia in Patients Undergoing Holmium Laser Prostatectomy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorAnkara City Hospital Bilkent

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • intraoperative body temperature

    Diagnostic test

    Body temperature measurement with esophageal probe

Treatment groups

106 Participants
are divided into 2 treatment groups
Group A: Prewarming GroupExperimental treatment 1 intervention
Group B: Control GroupOther 1 intervention

Trial outcomes

Primary outcomes

1

Time to onset of intraoperative hypothermia.

Time to develop intraoperative hypothermia (when body temperature drops below 36°C)

Time frame
intraoperatively

Secondary outcomes

1

Hemodynamic parameters

heart rate

Time frame
intraoperatively
2

Volume of irrigation fluid used

Volume of irrigation fluid used

Time frame
intraoperatively
3

Changes in body temperature

Changes in preoperative and intraoperative body temperature

Time frame
intraoperatively
4

Hemodynamic parameters

mean arterial pressure

Time frame
intraoperatively

Other outcomes

Sponsors and contacts

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