Evaluation of Synchrony in the Post-operative Patient

Not Applicable

Completed

• Conditions: Patient-ventilator Asynchronism
• Interventions: Device: MAQUET SERVOi ventilator; Device: MAQUET SERVOi ventilator with Edi Catheter

• Registration Number: NCT01771341
• Lead Sponsor: Hospices Civils de Lyon

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-02
• Study First Submitted: 2012-06-15
• Study First Submitted QC: 2013-01-16
• Study First Posted: 2013-01-18
• Primary Completion: 2014-12
• Study Completion: 2014-12
• Status Verified: 2015-01
• Last Update Submitted: 2015-01-21
• Last Update Posted: 2015-01-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 29

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Pressure support	MAQUET SERVOi ventilator	-
NAVA	MAQUET SERVOi ventilator with Edi Catheter	-

Primary Outcome Measures

Name	Time	Method
Asynchrony index (AI)	8 hours	Number of asynchrony events/total respiratory rate

Secondary Outcome Measures

Name	Time	Method
PaO2/FiO2 ratio	8 hours	ratio of partial pressure arterial oxygen and fraction of inspired oxygen

Trial Locations

Locations (1)

Hospices Civils de Lyon- Centre Hospitalier Lyon Sud; 🇫🇷 Pierre Bénite, France