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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01858727
Other study ID # ESM0606
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2018
Est. completion date July 1, 2019

Study information

Verified date October 2019
Source Ankara Diskapi Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date July 1, 2019
Est. primary completion date February 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 50 Years to 85 Years
Eligibility 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)

Study Design


Intervention

Other:
forced air warming group
30 minutes before the preoperative will use forced air warming
control group
do not heating group

Locations

Country Name City State
Turkey Diskapi Teaching and Research Hospital Ankara Altindag

Sponsors (1)

Lead Sponsor Collaborator
Ankara Diskapi Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other To assess patient satisfaction patient satisfaction scale (using a Likert scale type (range, 1 to 7) verbally administered questionnaire for patient satisfaction) 12 hours
Primary Perioperative measurements of core temperature (centigrade ° C) After 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. 2-3 hours
Secondary Evaluation of hemodynamic variables (arterial blood pressure) systolic blood pressure (SBP) in mmHg, diastolic blood pressure (DBP) in mmHg, mean arterial pressure (MAP) in mmHg will be measured. 2-3 hours
Secondary Evaluation of hemodynamic variables (heart rate) heart rate (HR) in beats per minute will be measured. 2-3 hours
Secondary Number of patients with postoperative shivering After the operation patients will be admitted to the PACU. Here, postoperative shivering will be measured and graded by visual inspection. 2-3 hours
See also
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