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

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

Treatments tested in this trial

  • intraoperative body temperature

Treatment groups

106 Participants
are divided into 2 treatment groups

Locations

1
Ankara City Hospital Bilkent Ankara Turkey (Türkiye)

Sponsors and collaborators

Ankara City Hospital Bilkent

Lead sponsor