Ventilation in Cardiac Surgery

International Multicentre Observational Trial of Perioperative Ventilatory Management in Cardiac Surgery

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT03255356

Acronym

VENICE

Enrollment

1000

Registered

2017-08-21

Start date

2017-11-01

Completion date

2017-12-31

Last updated

2017-08-21

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

Conditions

Anesthesia, General, Bypass, Cardiopulmonary, Respiration, Artificial, Respiratory Complication

Keywords

Postoperative pulmonary complications, Protective mechanical ventilation, Alveolar lung recruitment manoeuvres, Cardiac Surgery Procedures

Brief summary

The purpose of this study is to evaluate prospectively ventilatory practices in the perioperative cardiac surgery period.

Detailed description

This is a International Multicentre Observational Trial on all adult cardiac surgery patients with cardiopulmonary bypass (CPB).

Interventions

OTHERSurvey

An anonymised questionnaire will be answered for each includable consecutive patient after verifying the absence of exclusion criteria.

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* All consecutive cardiac surgery patients with CPB during one predefined period, * Elective or urgent surgery as defined by EuroSCORE2.

Exclusion criteria

* Refusal of consent, * Pregnant women, * Age \< 18 years, * Heart transplant, ECLS, ventricular assist * Emergency or salvage surgery as defined by EuroSCORE2

Design outcomes

Primary

Measure	Time frame	Description
incidence of use prophylactic protective mechanical ventilation defined with with low tidal volume (6 to 8 ml / kg based on the ideal body weight)	1 day	percent

Secondary

Measure	Time frame	Description
incidence of using positive end-expiratory pressure	1 day	(PEEP)\> 5 cmH2O
incidence of using at least 2 alveolar lung recruitment manoeuvres	1 day	percent
incidence of using a protective ventilation bundle combining prophylactic protective mechanical ventilation and at least 2 alveolar recruitment manoeuvres	1 day	percent
incidence of postoperative pulmonary complications	1 month postoperatively	percent

Countries

Belgium, Brazil, Czechia, France, Germany, Italy, Japan, Netherlands, Norway, Poland

Contacts

Primary ContactMarc-Olivier Fischer, MD, PhD

fischer-mo@chu-caen.fr+33 2 31 06 31 06

Backup ContactJennifer Brunet, MD

brunet-j@chu-caen.fr33 2 31 06 31 06

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026