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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05126524
Other study ID # NR-2021-01
Secondary ID
Status Completed
Phase
First received
Last updated
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
Health authority
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

Study Design


Related Conditions & MeSH terms


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
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