Pre-warmed Intravenous Fluids and Monitored Anesthesia Care

Effect of Pre-warmed Intravenous Fluids on the Early Outcomes After Ambulatory Surgery Under Monitored Anesthesia Care

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01722955

Enrollment

Registered

2012-11-07

Start date

2012-09-30

Completion date

2014-11-30

Last updated

2014-11-19

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

Conditions

Hypothermia

Keywords

Prewarmed fluid, monitored anesthesia care, core body temperature, anesthetic satisfaction

Brief summary

The aim of the study is to compare effect of pre-warmed intravenous fluids on the early outcomes in ambulatory patients undergoing monitored anesthesia care.

Detailed description

Monitored anesthesia care (MAC) has been increasing in fast track anesthesia for ambulatory or outpatient surgery. MAC provides lower anesthetic agents than general anesthesia, however it has been shown to result high anesthetic complication rate because of negligent monitoring. Therefore, aim of this study is to investigate the effect of pre-warmed intravenous fluids on the core body temperature and the early outcomes.

Interventions

OTHERPre-warmed fluids

IV fluid will be stored at 41℃ set hot cabinet for 8hours

OTHERRoom temperature fluids

Room temperature fluid will be stored at ambient temperature

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender

FEMALE

Age

20 Years to 70 Years

Healthy volunteers

Inclusion criteria

* 20years to 70years old female patients undergoing urinary incontinence surgery under monitored anesthesia care.

Exclusion criteria

* Preoperative tympanic membrane temperature \>38 or \< 36 * End stage heart failure or renal failure * Otitis media

Design outcomes

Primary

Measure	Time frame	Description
Tympanic membrane temperature	30min after anesthetic induction	Preoperative dehydration will be supplemented with 10ml/kg of lactate Ringer's solution at the beginning of the anesthetic induction. 30 min after anesthetic induction is nearly after administering the fixed volume.

Secondary

Measure	Time frame	Description
Postoperative chilling and shivering	on arrival at the postanesthetic care unit ( 1hour after the anesthetic induction)	Degree of chilling and shivering will be evaluated at the postanesthesia care unit after the surgery.

Countries

South Korea

Outcome results

None listed

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