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Correlation of Survival in Puerperae by Electrical Impedance Tomography

NCT03715647 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2018-11-06

No results posted yet for this study

Summary

Introduction: Electrical Impedance Tomography (TIE) consists of an equipment that enables the visualization / quantification in real time of the regional distribution of ventilation and pulmonary perfusion, as well as of ventilatory mechanics. Used on the edge of the bed, it is easy to move, non-invasive, allowing a momentary or continuous assessment, guiding the conduct in a safe and precise way through the electrical impedance technology. It is important to note that, in addition to ensuring the efficacy of the patient's behavior, the TIE supports the most diverse types of studies to be performed. These include those based on the effectiveness of the use of the method in the most diverse pulmonary dysfunctions, in the adjustment of the mechanical ventilation and in the average time of hospitalization. Objective: To evaluate the pulmonary function of patients in invasive mechanical ventilation through SIT. Method: This research was carried out in compliance with the National Health Council's Guidelines for Research Involving Human Beings (466/12). The study was a prospective longitudinal clinical-experimental type in which all patients (occasional sampling) used mechanical ventilation and were hospitalized in the Adult Intensive Care Unit (ICU) of the Santa Casa de Misericórdia Foundation of Pará, and they developed sepsis with pulmonary repercussions; (DEHG) / HELLP Syndrome and Adult Respiratory Distress Syndrome (ARDS) and who met the inclusion criteria were evaluated and monitored with TIE to perform ventilatory therapy according to the research objectives. The research was carried out in the city of Belém, in the state of Pará, in the adult ICU of the FSCMP. As inclusion criterion, the patient should be in the FSCMP adult Intensive Care Unit (ICU), under mechanical invasive ventilation, previously authorized by the family through the Informed Consent Form to participate in the study.

Conditions

  • Postpartum Period
  • Sepsis
  • Respiratory Distress Syndrome,Adult
  • HELLP Syndrome

Interventions

OTHER

Sepsis

Evaluation and monitoring with Electrical Impedance Tomography in order to conduct ventilatory therapy.

OTHER

HELLP Syndrome

Evaluation and monitoring with Electrical Impedance Tomography in order to conduct ventilatory therapy.

OTHER

Respiratory Distress Syndrome Adult

Evaluation and monitoring with Electrical Impedance Tomography in order to conduct ventilatory therapy.

Sponsors & Collaborators

  • Santa Casa de Misericórdia do Pará

    collaborator UNKNOWN

  • Amazon University

    lead OTHER

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2017-12-31
Completion
2018-06-30

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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 NCT03715647 on ClinicalTrials.gov