Evaluation of Synchrony in the Post-operative Patient (SYNCHRONY)

Civil Hospices of Lyon

Status: Completed

Conditions: Patient-ventilator Asynchronism

Treatments: Device: MAQUET SERVOi ventilator; Device: MAQUET SERVOi ventilator with Edi Catheter

Study type: Interventional

Funder types: Other

Identifiers

NCT01771341

2010.646

Details and patient eligibility

About

Neurally adjusted ventilatory support improved synchronization in the medical patient. However no data are available in the postoperative patient.

This way the investigators designed a prospective randomized cross over trial to evaluate this issue in the abdominal post-operative patient.

Enrollment: 29 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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29 participants in 2 patient groups, including a placebo group

Pressure support

Placebo Comparator group

Treatment:

Device: MAQUET SERVOi ventilator

NAVA

Experimental group

Treatment:

Device: MAQUET SERVOi ventilator with Edi Catheter