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Not yet recruiting NCT06847659

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

No phase Interventional Prewarming Holmium Laser Prostate Surgery Hypothermia Following Anesthesia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: intraoperative body temperature.
Who it may be relevant to
Registry conditions: Prewarming, Holmium Laser Prostate Surgery, Hypothermia Following Anesthesia. Basic parameters: from 18 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

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

Overview

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.

Interventions

  • Diagnostic test intraoperative body temperature
    Body temperature measurement with esophageal probe

Primary outcome measures

  • Time to onset of intraoperative hypothermia. [Time frame: intraoperatively]
Secondary outcome measures (5)
  • Hemodynamic parameters [Time frame: intraoperatively]
  • Volume of irrigation fluid used [Time frame: intraoperatively]
  • Changes in body temperature [Time frame: intraoperatively]
  • Hemodynamic parameters [Time frame: intraoperatively]
  • respiratory parameter [Time frame: intraoperatively]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Diagnostic

Study locations

Turkey (Türkiye) · 1 center
  • Ankara City Hospital Bilkent — Ankara

Identifiers

NCT: NCT06847659 · TABED1-24-841

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗