Evaluation of Synchrony in the Post-operative Patient

• Register: ClinicalTrials.gov
• Last refreshed on: 19 February 2015
• Main ID: NCT01771341
• Date of registration: 15/06/2012
• Prospective Registration: No
• Primary sponsor: Hospices Civils de Lyon
• Public title: Evaluation of Synchrony in the Post-operative Patient SYNCHRONY
• Scientific title: Evaluation of Synchrony in the Post-operative Patient (NAVA vs Pressure Support)
• Date of first enrolment: February 2012
• Target sample size: 29
• Recruitment status: Completed
• URL: http://clinicaltrials.gov/show/NCT01771341
• Study type: Interventional
• Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science
• Phase: N/A

Countries of recruitment

France

Contacts

• Name: Florent WALLET, MD
• Affiliation: Hospices Civils de Lyon

Key inclusion & exclusion criteria

Inclusion Criteria:

- adult > 18 yr-old

- abdominal post-operative patient

- able to trigger the ventilator

Exclusion Criteria:

- infant

- pregnancy

- esophageal surgery

- recent esophageal variceal bleeding



Age minimum: 18 Years
Age maximum: N/A
Gender: Both

Health Condition(s) or Problem(s) studied

Patient-ventilator Asynchronism

Intervention(s)

Device: MAQUET SERVOi ventilator with Edi Catheter

Device: MAQUET SERVOi ventilator

Primary Outcome(s)

Asynchrony index (AI) [Time Frame: 8 hours]

Secondary Outcome(s)

PaO2/FiO2 ratio [Time Frame: 8 hours]

Secondary ID(s)

2010.646

Source(s) of Monetary Support

Please refer to primary and secondary sponsors