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Prospective Randomized Controlled Trial Comparing Adaptive-support Ventilation with INTELLiVENT-ASV after Cardiac Surgery

Prospective Randomized Controlled Trial Comparing Adaptive-support Ventilation with INTELLiVENT-ASV on weaning patients cardiac sugery patients.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001505
Enrollment
Unknown
Registered
2014-09-21
Start date
2012-10-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

coronary artery disease

Interventions

Two groups:INTELLiVENT-ASV ventilation mode, Adaptive-support ventilation mode versus Physician-led weaning

Sponsors

Dept. of Anesthesia and Intensive Care
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Haemodynamically stable patients aged over 18 years, receiving mechanical ventilation support after elective coronary arterial bypass grafting will be consecutively included. Written informed consent will be obtained from each patient before surgery.

Exclusion criteria

Exclusion criteria: Preoperative exclusion criteria: patients older than 80 years or younger than 18 years, acute or chronic obstructive pulmonary disease (primary indication for ventilation), and concomitant valvular and/or aortic surgeries, major organ failure (liver disease, renal failure), history of seizure or stoke are excluded preoperatively. Postoperative exclusion criteria: Severe early postoperative haemorrhage (chest tube drainage >500 ml/h), surgical complications needing reoperation, myocardial ischemia (ST-segment depression) lasting more than 30 min, postoperative cardiac failure necessitating high-dose inotropes or intra aortic balloon pump; refractory hypoxemia (ratio of arterial oxygen tension [PaO2] to fraction of inspired oxygen [FIO2] <150 mmHg)?

Design outcomes

Primary

MeasureTime frame
Duration of mechanical ventilation during intensive care unit stay;Frequency of manual setting during intensive care unit stay;Frequency of alarms during intensive care unit stay;

Secondary

MeasureTime frame
Hospital length of stay during hostipal stay;Reintubation rate during intensive care unit stay;Tidal volume within 10 minutes after weaning;Respiratory ratr within 10 minutes after weanin;

Countries

China

Contacts

Public ContactPui-Nga Patricia LEUNG
leungyaya@cuhk.edu.hk+852 2632 3155

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026