Comparison of the effects of dexmedetomidine and propofol on hypothermia during spinal anesthesia

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005395

Enrollment

Registered

2020-09-09

Start date

2020-09-15

Completion date

Unknown

Last updated

2021-01-06

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

Conditions

None listed

Interventions

Drug : After spinal anesthesia, when the level of nerve block is confirmed, intravenous infusion of a sedative (dexmedetomidine or propofol) is started according to the group assigned by randomization

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for surgery under spinal anesthesia 2. American Society of Anesthesiologist Patient Status I~III (I is a normal healthy patient, II is patient with mild systemic disease and III is patient with moderate systemic disease). 3. 19 ~ 70 year old

Exclusion criteria

Exclusion criteria: - Conversion to general anesthesia before the end of surgery - Core temperature measured in the preoperative ward = 37.6°C or < 36.0°C - Obesity (Body mass index >35 kg/m2) - Uncontrolled diabetes - Abnormal thyroid function - Contraindications to spinal anesthesia - Infection - Psychiatric patients - Patients with cognitive impairment

Design outcomes

Primary

Measure	Time frame
maximum temperature change (= baseline temperature - the lowest temperature)	—

Secondary

Measure	Time frame
incidence of hypothermia (core temperature < 36 °C)	—

Countries

Korea, Republic of

Contacts

Public ContactTae-Yun Sung

Konyang University Hospital

Outcome results