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Effect of preoperative warming and use of phenylephrine infusion on postoperative hypothermia in anesthetized adult patients.

Effect of short-term preoperative warming and combined use of phenylephrine infusion on postoperative hypothermia in anesthetized adult patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0006599
Enrollment
58
Registered
2021-09-27
Start date
2021-10-06
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

None listed

Interventions

Drug, Medical Device : All subjects are evaluated for thermal comfort after measuring their body temperature upon arrival at the entrance to the operating room. The study subjects of the active contro

Sponsors

Konyang University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged 19 or older and under 80 years of age undergoing urology surgery under general anesthesia 2. Patients who are class 1,2 of American Society of Anesthesiologists physical status classification.

Exclusion criteria

Exclusion criteria: - Body temperature measured in the ward before surgery is 37.6°C or higher or less than 36.0°C - Obesity (body mass index >35kg/m2) - Severe endocrine, cardiovascular, or respiratory disease - Psychiatric history and cognitive impairment - Unstable hemodynamic signs upon admission to surgery [bradycardia (heart rate 120 beats/min), hypertension (systolic blood pressure > 180 mmHg), hypotension (systolic blood pressure < 90 mmHg)] - When the time from induction of anesthesia to termination of anesthesia is less than 1 hour

Design outcomes

Primary

MeasureTime frame
incidence rate of postoperative hypothermia

Secondary

MeasureTime frame
the difference of postoperative core temperature

Countries

Korea, Republic of

Contacts

Public ContactSung-Ae Cho

Konyang University Hospital

whtjddo89@gmail.com+82-42-600-9301

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026