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EASiVENT Study Comparing INTELLiVENT-ASV vs Non Automated Ventilation in Adult ICU Patients

NCT04400643 · Status: TERMINATED · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2024-10-23

Study results available
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Summary

The purpose of the study is to assess the safety and efficacy of INTELLiVENT-ASV (Adaptive Support Ventilation) in adult ICU patients comparing to non automated ventilation.

Conditions

  • Acute Respiratory Failure
  • Coma
  • Acute Respiratory Distress Syndrome (ARDS)
  • Chronic Obstructive Pulmonary Disease (COPD)
  • Obesity

Interventions

DEVICE

INTELLiVENT-ASV

INTELLiVENT-ASV is software accessory that automatically adjust ventilation and oxygenation variables to keep the patient within clinician-set target ranges.

DEVICE

Non-automated ventilation

In conventional ventilation modes, clinicians adjust and modify the oxygenation and ventilation parameters manually.

Sponsors & Collaborators

  • Hamilton Medical AG

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-20
Primary Completion
2022-07-18
Completion
2022-07-18

Countries

  • Portugal

Study Locations

More Related Trials

Entities

Diseases

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 NCT04400643 on ClinicalTrials.gov