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Transcutaneous Diaphragm Electrical Stimulation in Critically Ill Patients

NCT04171024 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2022-08-04

No results posted yet for this study

Summary

This study evaluates the effect of a transcutaneous electrical stimulation in critically ill patients compared to a sham electrical stimulation to decrease the incidence of diaphragm dysfunction before mechanical ventilation weaning.

Conditions

  • Critical Illness
  • Mechanical Ventilation
  • Intensive Care Unit

Interventions

DEVICE

Sham electrical stimulation

A non invasive sham diaphragm electrical stimulation using transcutaneous thoracic probes

DEVICE

Transcutaneous diaphragm electrical stimulation

A non invasive diaphragm electrical stimulation using transcutaneous thoracic probes

Sponsors & Collaborators

  • Groupe Hospitalier du Havre

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2019-12-10
Primary Completion
2022-08-02
Completion
2022-08-03

Countries

  • France

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 NCT04171024 on ClinicalTrials.gov