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

Pulmonary Surgical Procedures Clinical Trial

— ARTIST  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05126524
• Other study ID #: NR-2021-01
• Status: Completed
• Start date: January 4, 2021
• Est. completion date: December 31, 2022

Study information

• Verified date: April 2023
• Source: Société Française d'Anesthésie et de Réanimation
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical 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 used in Video or Robot-assisted Thoracic Pulmonary Surgery within French teams.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 456
• Est. completion date: December 31, 2022
• Est. primary completion date: September 30, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Pulmonary Surgical Procedures

Intervention

Other:
• NO INTERVENTION
Observational study, no intervention performed

Locations

Country	Name	City	State
France	CHU d'Angers	Angers
France	Hôpital Privé d'Antony	Antony
France	Clinique de l'Infirmerie Protestante de Lyon	Caluire-et-Cuire
France	centre de Lutte Contre le Cancer Jean Perrin	Clermont-Ferrand
France	Chu Dijon	Dijon
France	CHU de Grenoble	La Tronche
France	Hôpital Marie Lannelongue	Le Plessis-Robinson
France	CHRU de Lille _Clinique Cardiothoracique et Vasculaire	Lille
France	CHU Limoges	Limoges
France	Centre Leon Bérard	Lyon
France	Hôpital Nord Marseille	Marseille
France	Hôpital Arnaud de Villeneuve	Montpellier
France	CHRU de Nancy	Nancy
France	CHU Nantes - Réa CTCV de l'HGR	Nantes
France	CHR d'ORLEANS	Orléans
France	Hôpital Bichat	Paris
France	Hôpital Européen Georges Pompidou	Paris
France	Hôpital TENON	Paris
France	Institut Mutualist Montsouris - Paris	Paris
France	CHU de Poitiers	Poitiers
France	Hôpital Privé Claude Galien	Quincy-Sous-Sénart
France	CHU de Rennes, Hôpital de Pontchaillou	Rennes
France	Polyclinique Saint Laurent	Rennes
France	CHU Charles Nicolle	Rouen
France	Centre Hospitalier de Toulon	Toulon
France	HIA Sainte-Anne - Toulon	Toulon

Sponsors (1)

Lead Sponsor	Collaborator
Société Française d'Anesthésie et de Réanimation

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic
Secondary	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	At least, 6 months after the publication of the SFAR / SFCTCV 2019 recommendations concerning this topic
Secondary	Epidemiology of perioperative morbidity and mortality	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