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Pulmonary Surgical ProceduresARTISTNCT05126524

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

An observational study of Pulmonary Surgical Procedures, run by Société Française d'Anesthésie et de Réanimation at 26 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Pulmonary Surgical Procedures
How many people
456 participants
Where
26 sitesFrance
Study dates
4 Jan 2021to 31 Dec 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patients with planned wedge surgery or lobectomy with Video or Robot assisted surgery

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

26 sites in 1 country.

26 sites in 1 country

France26 sites
  • CHU d'Angers

    Angers, 49100

  • Hôpital Privé d'Antony

    Antony, 92160

  • Clinique de l'Infirmerie Protestante de Lyon

    Caluire-et-Cuire, 69300

  • centre de Lutte Contre le Cancer Jean Perrin

    Clermont-Ferrand, 63011

  • Chu Dijon

    Dijon, 21000

  • CHU de Grenoble

    La Tronche, 38700

  • Hôpital Marie Lannelongue

    Le Plessis-Robinson, 92350

  • CHRU de Lille _Clinique Cardiothoracique et Vasculaire

    Lille, 59000

  • CHU Limoges

    Limoges, 87000

  • Centre Leon Bérard

    Lyon, 69008

  • Hôpital Nord Marseille

    Marseille

  • Hôpital Arnaud de Villeneuve

    Montpellier, 34295

  • CHRU de Nancy

    Nancy, 54511

  • CHU Nantes - Réa CTCV de l'HGR

    Nantes, 44093

  • CHR d'ORLEANS

    Orléans, 45100

  • Institut Mutualist Montsouris - Paris

    Paris, 75014

  • Hôpital Européen Georges Pompidou

    Paris, 75015

  • Hôpital Bichat

    Paris, 75018

  • Hôpital TENON

    Paris, 75020

  • CHU de Poitiers

    Poitiers, 83021

  • Hôpital Privé Claude Galien

    Quincy-sous-Sénart, 91480

  • CHU de Rennes, Hôpital de Pontchaillou

    Rennes, 35 033

  • Polyclinique Saint Laurent

    Rennes, 35700

  • CHU Charles Nicolle

    Rouen, 76000

  • Centre Hospitalier de Toulon

    Toulon, 83000

  • HIA Sainte-Anne - Toulon

    Toulon, 83800

Other trials in France

About this study

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.

Read the 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.

Being tested
NO INTERVENTION
Keywords
Loco-regional Anaesthesia, Video or Robot-assisted Thoracic Pulmonary Surgery, ARTIST, SFAR

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • NO INTERVENTIONOther

    Observational study, no intervention performed

Study groups in NCT05126524
Study groupRoleWhat they receive
Loco-regional Anaesthesia in Video or Robot-assisted Thoracic Pulmonary SurgeryPatients with loco-regional Anaesthesia in Video or Robot-assisted Thoracic Pulmonary Surgery are eligible for this study
Receives: Other: NO INTERVENTION

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. to assess the incidence of locoregional anesthesia in video or robot-assisted thoracic pulmonary surgery

    Information concerning locoregional anesthesia in video or robot-assisted thoracic are recorder in the CRF

    Measured: At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic

Secondary outcomes (2)
  1. Epidemiology of anaesthesia management during Video or Robot-assisted Thoracic Pulmonary Surgery

    Information concerning locoregional anesthesia in video or robot-assisted thoracic are recorder in the CRF

    Measured: At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic

  2. Epidemiology of perioperative morbidity and mortality

    nformation concerning lmorbidity and mortality are recorder in the CRF

    Measured: At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Nov 2021
  2. Study start4 Jan 2021
  3. Primary completion30 Sep 2022
  4. Study completion31 Dec 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
456 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05126524
Sponsor's protocol ID
NR-2021-01
Acronym
ARTIST
Status last verified
Apr 2023
First submitted
8 Nov 2021
Last updated
12 Apr 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Le Gac G, Mansour A, Richard de Latour B, Casez-Brasseur, Coves R, Desbordes J, Dransart-Raye O, Dufour G, Gayraud G, Gil C, Gouel-Cheron A, Guerci P, Huette P, Kerforne T, Lebreton C, Lemoine A, Maupain O, Parent C, Piclet J, Pihan F, Prieur S, Rineau E, Roux F, Selim J, Thes J, Beloeil, Nesseler N; SFAR Research Network. Regional anaesthesia in Video or Robot assisted thoracic surgery: A French multicentre prospective observational cohort study (ARTIST study). Anaesth Crit Care Pain Med. 2026 Jul;45(4):101830. doi: 10.1016/j.accpm.2026.101830. Epub 2026 Mar 22.

    PubMed 41875998

Questions about this trial

What is this clinical trial studying?

An observational study of Pulmonary Surgical Procedures, run by Société Française d'Anesthésie et de Réanimation at 26 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 26 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05126524, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Apr 2023.

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