Loco-regional Anaesthesia in Video or Robot-assisted Thoracic Pulmonary Surgery (ARTIST)

April 11, 2023 updated by: Société Française d'Anesthésie et de Réanimation

Currently, there is no data on the part and type of Loco-regional Anaesthesia used for Video or Robot-assisted Thoracic Pulmonary Surgery.

The aim of this epidemiological study is to identify, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations, the proportion and type of Loco-regional Anaesthesia used in Video or Robot-assisted Thoracic Pulmonary Surgery within French teams.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Currently, there is no data on the part and type of Loco-regional Anaesthesia used for Video or Robot-assisted Thoracic Pulmonary Surgery. The experience and habits of each team taking charge of the perioperative period seem to be the determining factors for the achievement of one type of Loco-regional Anaesthesia over another.

The aim of this epidemiological study is to identify, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations, the proportion and type of Loco-regional Anaesthesia used in Video or Robot-assisted Thoracic Pulmonary Surgery within French teams.

Study Type

Observational

Enrollment (Actual)

456

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Angers, France, 49100
        • CHU d'Angers
      • Antony, France, 92160
        • Hopital Prive d'Antony
      • Caluire-et-Cuire, France, 69300
        • Clinique de l'Infirmerie Protestante de Lyon
      • Clermont-Ferrand, France, 63011
        • Centre de Lutte Contre le Cancer Jean PERRIN
      • Dijon, France, 21000
        • CHU Dijon
      • La Tronche, France, 38700
        • Chu de Grenoble
      • Le Plessis-Robinson, France, 92350
        • Hopital Marie Lannelongue
      • Lille, France, 59000
        • CHRU de Lille _Clinique Cardiothoracique et Vasculaire
      • Limoges, France, 87000
        • CHU Limoges
      • Lyon, France, 69008
        • Centre léon bérard
      • Marseille, France
        • Hôpital Nord Marseille
      • Montpellier, France, 34295
        • Hopital Arnaud de Villeneuve
      • Nancy, France, 54511
        • CHRU de NANCY
      • Nantes, France, 44093
        • CHU Nantes - Réa CTCV de l'HGR
      • Orléans, France, 45100
        • CHR d'Orléans
      • Paris, France, 75015
        • Hopital Europeen Georges Pompidou
      • Paris, France, 75020
        • Hopital Tenon
      • Paris, France, 75018
        • Hôpital Bichat
      • Paris, France, 75014
        • Institut Mutualist Montsouris - Paris
      • Poitiers, France, 83021
        • Chu de Poitiers
      • Quincy-Sous-Sénart, France, 91480
        • Hôpital Privé Claude Galien
      • Rennes, France, 35700
        • Polyclinique Saint Laurent
      • Rennes, France, 35 033
        • CHU de Rennes, Hopital de Pontchaillou
      • Rouen, France, 76000
        • CHU Charles Nicolle
      • Toulon, France, 83000
        • Centre Hospitalier de Toulon
      • Toulon, France, 83800
        • HIA Sainte-Anne - Toulon

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Patients with planned wedge surgery or lobectomy with Video or Robot assisted surgery

Description

Inclusion Criteria:

  • Male or female aged 18years and over
  • Wedge surgery or lobectomy planned with Video or Robot-assisted surgery.
  • non-opposition of the patient to participating in the research

Exclusion Criteria:

  • Patient's refusal to use his data for research
  • Emergency surgery
  • Surgery with planned thoracotomy
  • Contraindications to performing locoregional anesthesia
  • Individual deprived of liberty or placed under the authority of a tutor

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Loco-regional Anaesthesia in Video or Robot-assisted Thoracic Pulmonary Surgery
Patients with loco-regional Anaesthesia in Video or Robot-assisted Thoracic Pulmonary Surgery are eligible for this study
Other: NO INTERVENTION
Observational study, no intervention performed

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
to assess the incidence of locoregional anesthesia in video or robot-assisted thoracic pulmonary surgery
Time Frame: At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic
Information concerning locoregional anesthesia in video or robot-assisted thoracic are recorder in the CRF
At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Epidemiology of anaesthesia management during Video or Robot-assisted Thoracic Pulmonary Surgery
Time Frame: At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic
Information concerning locoregional anesthesia in video or robot-assisted thoracic are recorder in the CRF
At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic
Epidemiology of perioperative morbidity and mortality
Time Frame: At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic
nformation concerning lmorbidity and mortality are recorder in the CRF
At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Société Française d'Anesthésie et de Réanimation

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 4, 2021

Primary Completion (Actual)

September 30, 2022

Study Completion (Actual)

December 31, 2022

Study Registration Dates

First Submitted

November 8, 2021

First Submitted That Met QC Criteria

November 8, 2021

First Posted (Actual)

November 19, 2021

Study Record Updates

Last Update Posted (Actual)

April 12, 2023

Last Update Submitted That Met QC Criteria

April 11, 2023

Last Verified

April 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • NR-2021-01

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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