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Pre-warmed Intravenous Fluids and Monitored Anesthesia Care

NCT01722955 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2014-11-19

No results posted yet for this study

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.

Conditions

  • Hypothermia

Interventions

OTHER

Pre-warmed fluids

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

OTHER

Room temperature fluids

Room temperature fluid will be stored at ambient temperature

Sponsors & Collaborators

  • Samsung Medical Center

    lead OTHER

Principal Investigators

  • Myung Hee Kim, MD,PhD · Samsung MC

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-09-30
Primary Completion
2014-11-30
Completion
2014-11-30

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01722955 on ClinicalTrials.gov