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Airflow systems in the operating rooms and the heat loss of patients during surgery.

Are the operating rooms with laminar airflow systems a risk for inadvertent perioperative hypothermia during ureterorenoscopic lithotripsy under spinal anesthesia? A prospective randomized clinical trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180324039145N5
Enrollment
100
Registered
2018-11-02
Start date
2018-12-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Inadvertent perioperative hypothermia. Hypothermia following anesthesia

Interventions

Intervention 1: Intervention group: Patients who will undergo ureterorenoscopic lithotripsy under spinal anesthesia, determined according to randomization, will be taken to the operating rooms with la

Sponsors

Department of Anaesthesiology and Reanimation, Ahi Evran University Faculty of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: The patients who will be applied ureterorenoscopic surgery under spinal anesthesia The patients who ASA (American Society of Anesthesiologists) score I-II The patients who in the 18-65 age group The patients who with the body mass index (BMI) between 18.5-29.9

Exclusion criteria

Exclusion criteria: The patients who treated for hypothyroid or hyperthyroid The patients who treated for corticoadrenal insufficiency The patients who treated for hypertension or arrhythmia The patients who treated for hypothermia during preoperative period.

Design outcomes

Primary

MeasureTime frame
To detect the change between the preoperative temperature and the temperature measured each fifteen-minutes during the ureterorenoscopic lithotripsy (?T). Timepoint: every fifteen-minutes during the ureterorenoscopic lithotripsy, until the end of the operation. Method of measurement: The tympanic membrane temperature of patients will be measured with Braun IRT6520.

Countries

Turkey

Contacts

Public ContactRecai Dagli

Department of Anaesthesiology and Reanimation, Ahi Evran University Faculty of Medicine

recai.dagli@ahievran.edu.tr+90 386 213 45 15

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 13, 2026