Comparative Study on Minimally Invasive Removal of Lung Cancer (LARCS)
Descrizione riassuntiva dello studio
In early-stage lung cancer, cancer cells are removed using minimally invasive surgical procedures to treat the cancer. All individuals undergoing such surgery can participate in this study.
In our research project, we aim to investigate recovery and quality of life after a minimally invasive surgical procedure for the treatment of early-stage lung cancer. To do this, we would like to collect information to better understand how the treatment you receive affects you.
The surgeon will perform the minimally invasive procedure using a robotic or video-assisted surgical device as usual. The surgical instruments used are not experimental, and the procedures performed with them are also not experimental.
The study team will collect some data about you as well as your health status before, during, and after the surgery. Additionally, data regarding the surgery itself will be recorded (e.g., details of the procedure and clinical measurements).
If you decide to participate, you will need to complete 3 quality of life questionnaires before the surgery, after discharge from the hospital, and 1 month, 3 months, and 6 months after the surgery.
Your participation in the study ends after completing your 6-month questionnaire, and we will not collect any further data after that time.
(BASEC)
Intervento studiato
Minimally invasive procedures using a robotic or video-assisted surgical device for the treatment of lung cancer
(BASEC)
Malattie studiate
Lung Cancer
(BASEC)
- Patient diagnosed with non-small cell lung carcinoma at primary stage IA1-2 at the time of the procedure
- Patient planned for minimally invasive surgery for non-small cell lung carcinoma with da Vinci robotic-assisted surgery or VATs
- Age ≥ 18 years
(BASEC)
Criteri di esclusione
- Patients receiving lobectomy/segmentectomy as an emergency
- Patients for whom a bilobectomy or sleeve resection is planned
- Life expectancy < 12 months
(BASEC)
Luogo dello studio
Zurigo
(BASEC)
Sponsor
Intuitive Surgical Sàrl
(BASEC)
Contatto per ulteriori informazioni sullo studio
Persona di contatto in Svizzera
Marie Allouis
+33 786 480 495
Clinical.Affairs.Europe@clutterintusurg.comIntuitive Surgical
(BASEC)
Informazioni scientifiche
non disponibile
Nome del comitato etico approvante (per studi multicentrici solo il comitato principale)
Commissione etica Zurigo
(BASEC)
Data di approvazione del comitato etico
02.04.2026
(BASEC)
ID di studio ICTRP
non disponibile
Titolo ufficiale (approvato dal comitato etico)
Comparing Outcomes for Minimally Invasive Techniques for Anatomic Lung Resection for Cancer - A Prospective, Comparative, Non-randomized, Open Label Post-market Observational Cohort Study Within Europe (BASEC)
Titolo accademico
non disponibile
Titolo pubblico
non disponibile
Malattie studiate
non disponibile
Intervento studiato
non disponibile
Tipo di studio
non disponibile
Disegno dello studio
non disponibile
Criteri di inclusione/esclusione
non disponibile
non disponibile
Endpoint primari e secondari
non disponibile
non disponibile
Data di registrazione
non disponibile
Inclusione del primo partecipante
non disponibile
Sponsor secondari
non disponibile
Contatti aggiuntivi
non disponibile
ID secondari
non disponibile
Risultati-Dati individuali dei partecipanti
non disponibile
Ulteriori informazioni sullo studio
non disponibile
Risultati dello studio
Riepilogo dei risultati
non disponibile
Link ai risultati nel registro primario
non disponibile