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The Effect of Preoperative Warming on Postoperative Hypothermia

The Effect of Preoperative Warming on Postoperative Hypothermia in TURP Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01858727
Enrollment
36
Registered
2013-05-21
Start date
2018-11-01
Completion date
2019-07-01
Last updated
2019-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perioperative Hypothermia, Preventing Hypothermia

Keywords

forced-air, hypothermia, TUR-P surgery, core temperatures, prewarming, general anaesthesia

Brief summary

36 patients American society of anesthesiology (ASA) physical status I,II and III undergoing general anesthesia for elective transurethral resection of the prostate (TUR-P) surgery will be included in the study. Patients will be randomized into two groups; first group(control group) and second group (forced-air warming). Resistive heating will start when patients are transferred to the operating room table; forced-air warming will start before preoperative 30 minute.

Detailed description

The primary aim of this study was to compare the effect of prewarming on perioperative hypothermia in elderly patients undergoing TURP under general anesthesia. In addition, we aimed to evaluate the effects of prewarming on hemodynamic variables, PACU output time, tremor, patient comfort and satisfaction. The investigators plan to enroll 36 patients in 2 groups. Body temperature will be measured at the core temperature, hemodynamic variables. Shivering will be graded by visual inspection. Thermal discomfort scale, patient satisfaction will be evaluated. The investigators hypothesize will decrease the forced air prewarming incidence of perioperative hypothermia.

Interventions

OTHERforced air warming group

30 minutes before the preoperative will use forced air warming

OTHERcontrol group

do not heating group

Sponsors

Ankara Diskapi Training and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
50 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients aged 50-85 years undergoing general anesthesia for TURP surgery * ASA physical status I and III patients * Body mass index between 15 and 36 kg/m2 * General anesthesia time is 30-90 minutes

Exclusion criteria

* without written consent, * inadequate Turkish comprehension, * known impaired thermoregulation or thyroid disorders, * severe hypertension (systolic blood pressure \[SBP\]\>180 mmHg or diastolic blood pressure \[DBP\] \> 110 mmHg in the operating suite admission), * an angiotensin-converting enzyme inhibitor/angiotensin II receptor antagonist on the day of surgery, * secondary hypertension (e.g., renal artery stenosis, pheochromocytoma, Cushing's syndrome), * vascular disease, * poor cutaneous perfusion, * serious skin lesions * baseline temperature ≥37.5°C (degrees centigrade)

Design outcomes

Primary

MeasureTime frameDescription
Perioperative measurements of core temperature (centigrade ° C)2-3 hoursAfter the operation patients will be admitted to the PACU. Here, body temperature will be assessed and the incidence of hypothermic patients (body temperature \< 36°C)will be measured.

Secondary

MeasureTime frameDescription
Evaluation of hemodynamic variables (arterial blood pressure)2-3 hourssystolic blood pressure (SBP) in mmHg, diastolic blood pressure (DBP) in mmHg, mean arterial pressure (MAP) in mmHg will be measured.
Evaluation of hemodynamic variables (heart rate)2-3 hoursheart rate (HR) in beats per minute will be measured.
Number of patients with postoperative shivering2-3 hoursAfter the operation patients will be admitted to the PACU. Here, postoperative shivering will be measured and graded by visual inspection.

Other

MeasureTime frameDescription
To assess patient satisfaction12 hourspatient satisfaction scale (using a Likert scale type (range, 1 to 7) verbally administered questionnaire for patient satisfaction)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026