CompletedNCT03309280Updated Jan 27, 2020

Influence of Different Parameters on Extubation Time After Cardiac Surgery.

An observational study in Thoracic Surgery, sponsored by Astes. Completed at 1 site in Belgium. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-01-27.

Study summary

The aim of this study is to determine which factors could be at risk of delayed extubation after cardiac surgery.

Read the detailed description

The aim of this study is to determine which factors could be at risk of delayed extubation after cardiac surgery. Several parameters of ventilation and infusion were recorded during surgery. A statistical analysis will be performed to determine if one of many of these are significant. The investigator does not assign specific interventions to the study participants, so the present study is observational and not interventional.

Conditions studied

Thoracic Surgery

Who can participate

Ages eligible: 18 Years and older
Sexes eligible: All
Sampling method: Probability sample

Study population

All patients scheduled for cardiac surgery in the Saint-Luc Bouge hospital.

Inclusion criteria

All patients for elective cardiac surgery

Exclusion criteria

Exclusion Criteria:

Emergency procedures

Study design

Observational model: Cohort
Time perspective: Prospective
Enrollment: 132 participants (actual)
Patient registry: No

Groups and cohorts

Patient at risk for OSA scheduled for Cardiac surgery
Patients with a positive STOP-Bang and DES-OSA score (that means patients at risk for OSA)
Other: Duration of intubation · Diagnostic Test: Evolution of the renal function
Patient not at risk for OSA scheduled for Cardiac surgery
Patients with a negative STOP-Bang and DES-OSA score (that means patients not at risk for OSA)
Other: Duration of intubation · Diagnostic Test: Evolution of the renal function

Interventions

OtherDuration of intubation
Time between intubation in the operating room and exhumation in the Intensive Care Unit.
Diagnostic testEvolution of the renal function
Evolution of the renal function in the next two days

What researchers measure

Primary outcomes

Time of extubation
Time when extubation is performed
Time frame: 2 Days

Study locations

1 site

Clinique Saint-Luc de Bouge
Bouge, Namur 5004, Belgium

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

Registry details

Key details

Study ID: NCT03309280
Lead sponsor: Astes
Responsible party: Eric DEFLANDRE, MD, PhD, FCCP, FAHA (Head of Department, Astes) — Principal investigator
First posted: Oct 13, 2017
Start date: Oct 9, 2017
Primary completion: Apr 3, 2018
Completion: Jun 1, 2018
Last update: Jan 27, 2020

Study contacts

Eric Deflandre

principal investigator · Astes

Oversight

Data monitoring committee: No
FDA-regulated drug: No
FDA-regulated device: No

View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2020. You cannot join it, but the record below documents what was studied.

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Discussion

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