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Assessment of Plasma Lactate in Non-cardiac Surgery Monitoring by Transthoracic Echocardiography

NCT03103373 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2017-04-06

No results posted yet for this study

Summary

The study is a clinical trial, prospective and randomized of 60 patients of both genders, aged between 18 and 80 years, underwent major abdominal surgery. This study aims to compare plasma lactate levels in patients underwent major abdominal surgery (colectomy, gastrectomy, esophagectomy, pancreatectomy, Wertheim Meigs, liver and spleen surgeries) monitored by echocardiography or by conventional techniques (mean arterial pressure , Central venous pressure).

Conditions

  • Anesthesia

Interventions

DEVICE

Conventional monitor

Patients underwent non-cardiac surgery will be monitoring by regular monitors

DEVICE

Echocardiography

Patients will be monitoring by regular monitors plus echocardiography

Sponsors & Collaborators

  • Federal University of Juiz de Fora

    lead OTHER

Principal Investigators

  • Marcello F Salgado Filho, PhD · Federal University of Juiz de Fora

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-01
Primary Completion
2017-12-01
Completion
2018-01-01
FDA Device
Yes

Countries

  • Brazil

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 NCT03103373 on ClinicalTrials.gov