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

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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)

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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