The full closed loop ventilation mode Intellivent-ASV: user-friendly and effective mechanical ventilation in high risk postoperative patients on the intensive care unit.

The full closed loop ventilation mode Intellivent-ASV: user-friendly and effective mechanical ventilation in high risk postoperative patients on the intensive care unit. - 'POSiTIVE'-trial (POSToperative Intellivent VEntilation)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON45718

Enrollment

250

Registered

2017-06-16

Start date

2017-05-22

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intensive Care geneeskunde, postoperatieve mechanische ventilatie Postoperative mechanical ventilation and weaning. Mechanical ventilation after surgery.

Interventions

Fully closed loop ventilation

INTELLiVENT-ASV ventilation mode

- The intervention group will be mechanically ventilated with INTELLiVENT-ASV with Quickwean after surgery. - The control group will be mechanically ventilated based on the conventional method, cons

Conventional ventilation mode

Postoperative ventilation

Eligibility

Age

18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Age above 18 years of age. Informed consent. Body mass index of

Exclusion criteria

Exclusion criteria: Withdrawal of consent The patient with a medical history of a pneumonectomy or lobectomy. The patient wit acute respiratory distress syndrome after surgery. The patient with a medical history of COPD Gold 3 or 4. The patient is participating in another postoperative study performed on the intensive care. The patient is, preoperatively determined, eligible for a shorttrack postoperative treatment program on the Post Anesthesia Care Unit.

Design outcomes

Primary

Measure	Time frame
The effectiveness of INTELLiVENT-ASV compared to conventional mechanical ventilation: 1. Percentage of mechanical ventilation time in an optimal, acceptable or unacceptable zone for the first three hours of postoperative mechanical ventilation time after admission on the intensive care unit. 2. The number of successful extubations (without new intubation 35.5 ° C. User-friendliness of IntelliVent-ASV compared to conventional mechanical ventilation: 1. Based on the measurement of the number of interactions between the caregiver and the ventilator. 2. Survey and semistructured interviews of usability and acceptance for the caregivers.	—

Measure

Time frame

The effectiveness of INTELLiVENT-ASV compared to conventional mechanical ventilation: 1. Percentage of mechanical ventilation time in an optimal, acceptable or unacceptable zone for the first three hours of postoperative mechanical ventilation time after admission on the intensive care unit. 2. The number of successful extubations (without new intubation 35.5 ° C. User-friendliness of IntelliVent-ASV compared to conventional mechanical ventilation: 1. Based on the measurement of the number of interactions between the caregiver and the ventilator. 2. Survey and semistructured interviews of usability and acceptance for the caregivers.

—

Secondary

Measure	Time frame
The safety of INTELLiVENT-ASV compared to conventional mechanical ventilation: 1. Percentage of mechanical ventilation time with an oxygen saturation	—

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)