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Fluid Responsiveness in the Postoperative Patient: a Prospective Study

NCT02418663 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 245

Last updated 2015-05-15

No results posted yet for this study

Summary

The aim of this study is to determine the prevalence of Fluid Responsiveness (FR) (SV increases by at least 15% after Volume Expansion, VE) in postoperative patients admitted on a surgical ward after elective abdominal, thoracic and esophageal surgery

Conditions

  • Actual Impaired Fluid Volume

Interventions

DRUG

Fluid challenge (250 ml Lactated Ringer's solution)

When VE is prescribed to a patient, a fluid challenge of 250mL Lactated Ringer's solution will first be administered. The ccNexfin system will be used to predict FR (SV increases by at least 15% in response to a fluid challenge). The remaining amount of fluid ordered by the treating team will then be administered, and SV will again be measured. Additionally, a daily fluid challenge with 250mL of Lactated Ringer's will also be administered, with FR recorded as above

Sponsors & Collaborators

  • McGill University Health Centre/Research Institute of the McGill University Health Centre

    lead OTHER

Principal Investigators

  • Gabriele Baldini, MD, MSc · McGill University Health Centre/Research Institute of the McGill University Health Centre

Study Design

Allocation
NA
Purpose
SCREENING
Masking
TRIPLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2017-04-30
Completion
2017-06-30

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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 NCT02418663 on ClinicalTrials.gov