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Prospective Clinical Surveillance With Application of Trigger Tools in Critically Ill Patients

NCT03781713 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 1200

Last updated 2018-12-26

No results posted yet for this study

Summary

This study evaluates the impact of prospective clinical surveillance with the use of triggers to identify risk of adverse events with prompt adoption of interventions on the stabilization time of critically ill patients.

Conditions

  • Critical Illness

Interventions

OTHER

KDIGO

Interventions to prevent renal replacement therapy

OTHER

Delta SOFA

interventions to improve SOFA score

COMBINATION_PRODUCT

Hypoglycemia

Interventions to prevent new episodes of hypoglycemia in the next 24 hours

DRUG

Drug interaction risk D or X

Intervention in the therapeutic plan in order to avoid adverse drug reactions.

DRUG

Antimicrobial stewardship

Optimization of anticrobial therapy based on Gram stain, MALDI TOF, MIC and antimicrobial susceptibility

Sponsors & Collaborators

  • Hospital Sao Domingos

    lead OTHER

Principal Investigators

  • JOSE R AZEVEDO, MD. PhD · Hospital Sao Domingos

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-01
Primary Completion
2018-10-31
Completion
2018-12-10

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 NCT03781713 on ClinicalTrials.gov