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Clinical Trials/NCT06847659
NCT06847659Not yet recruitingNot Applicable

Comparison of the Effect of Prewarming on Intraoperative Hypothermia in Patients Undergoing HoLEP (Holmium Laser Prostatectomy) Surgery

Ankara City Hospital Bilkent1 site in 1 country106 target enrollmentStarted: March 1, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
106
Locations
1
Primary Endpoint
Time to onset of intraoperative hypothermia.

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Male patients aged 18 years and older
  • •Patients undergoing HoLEP surgery under general anesthesia
  • •Patients who consent to participate in the study

Exclusion Criteria

  • •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.

Arms & Interventions

Prewarming Group

Experimental

Patients will receive 10 minutes of 43°C forced-air warming and 41°C prewarmed intravenous fluid before surgery. Surgery will begin following the standard induction of general anesthesia once patients are in the operating room. An air blower set to 43°C will maintain patient warmth throughout the procedure.

Intervention: intraoperative body temperature (Diagnostic Test)

Control Group

Other

No prewarming will be applied. Surgery will begin following the standard induction of general anesthesia once patients are in the operating room. An air blower set to 43°C will maintain patient warmth throughout the procedure.

Intervention: intraoperative body temperature (Diagnostic Test)

Outcomes

Primary Outcomes

Time to onset of intraoperative hypothermia.

Time Frame: intraoperatively

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

Secondary Outcomes

  • Hemodynamic parameters(intraoperatively)
  • Volume of irrigation fluid used(intraoperatively)
  • Changes in body temperature(intraoperatively)
  • respiratory parameter(intraoperatively)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Betül Güven

Ankara City Hospital Bilkent

Ankara City Hospital Bilkent

Study Sites (1)

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