Impact of Extubation Location After Surgery on Perioperative Times

NCT ID: NCT06249659

Last Updated: 2024-02-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

756 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-09-01

Study Completion Date

2023-02-01

Brief Summary

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The additional time required to awaken a patient is one of the main reasons for not extubating him or her in the operating room (OR). Conversely, transferring an intubated patient to recovery room (RR), prolonging the duration of anesthesia and intubation, in a limited environment in human resources, may lead to increased complications' rates. Little is known about those time lengths and complications rates.

Detailed Description

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The additional time required to awaken a patient is one of the main reasons for not extubating him or her in the operating room (OR). Conversely, transferring an intubated patient to recovery room (RR), prolonging the duration of anesthesia and intubation, in a limited environment in human resources, may lead to increased complications' rates. Little is known about those time lengths and complications rates. The primary objective was to evaluate the additional OR occupancy time associated with awakening and extubation. Secondary objectives were to assess the rate of post-extubation complications and the need for ventilatory support. This was a prospective multicenter observational study involving intubated patients who underwent surgeries in the operating theatres of the Montpellier and Clermont-Ferrand university hospitals. Anesthesia teams were asked to complete a form including data related to the patient, surgical procedure, anesthesia procedure (induction and recovery) and the occurrence of any complications during the procedure. A multivariate analysis was conducted on the full cohort, using a propensity score (IPTW, inverse probability of treatment weighting) to account for imbalances between groups.

Conditions

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Anesthesia Intubation Surgery Extubation Respiratory Failure Complication,Postoperative

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Extubation in operative room

Patients are extubated in operative room after the end of surgery

Extubation in operative room

Intervention Type PROCEDURE

Extubation takes place in operative room

Extubation in post anesthesia care unit

Patients are extubated in post anesthesia care unit, after transfer from operative room

Extubation in post anesthesia care unit

Intervention Type PROCEDURE

Extubation takes place in post anesthesia care unit

Interventions

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Extubation in operative room

Extubation takes place in operative room

Intervention Type PROCEDURE

Extubation in post anesthesia care unit

Extubation takes place in post anesthesia care unit

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Adult (older than 18 years old)
* Patients admitted to any operative room of participating centre for a surgical or endoscopic procedure under general anaesthesia requiring endo-tracheal intubation
* Subjects must be covered by public health insurance
* Written informed consent from the patient or proxy (if present) before inclusion or once possible when patient has been included in a context of emergency.

Exclusion Criteria

* Patient extubated in intensive care unit
* Patient extubated during on-call hours (because of a reduced number of medical and paramedical staff)
* Patient extubated following cardiac surgery
* Refusal of study participation or to pursue the study by the patient
* Absence of coverage by the French statutory healthcare insurance system
* Protected person
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Montpellier

OTHER

Sponsor Role collaborator

University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Thomas Godet, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Clermont-Ferrand University Hospitals

Audrey De Jong, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Montpellier University Hospitals

Locations

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Clermont-Ferrand University Hospital

Clermont-Ferrand, , France

Site Status

Countries

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France

Other Identifiers

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IRB-MTP_2022_04_202201100

Identifier Type: -

Identifier Source: org_study_id

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