Comparative Study on Minimally Invasive Removal of Lung Cancer (LARCS)
Résumé de l'étude
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)
Intervention étudiée
Minimally invasive procedures using a robotic or video-assisted surgical device for the treatment of lung cancer
(BASEC)
Maladie en cours d'investigation
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)
Critères d'exclusion
- Patients receiving lobectomy/segmentectomy as an emergency
- Patients for whom a bilobectomy or sleeve resection is planned
- Life expectancy < 12 months
(BASEC)
Lieu de l’étude
Zurich
(BASEC)
Sponsor
Intuitive Surgical Sàrl
(BASEC)
Contact pour plus d'informations sur l'étude
Personne de contact en Suisse
Marie Allouis
+33 786 480 495
Clinical.Affairs.Europe@clutterintusurg.comIntuitive Surgical
(BASEC)
Informations scientifiques
non disponible
Nom du comité d'éthique approbateur (pour les études multicentriques, uniquement le comité principal)
Commission cantonale de Zurich
(BASEC)
Date d'approbation du comité d'éthique
02.04.2026
(BASEC)
Identifiant de l'essai ICTRP
non disponible
Titre officiel (approuvé par le comité d'éthique)
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)
Titre académique
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Titre public
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Maladie en cours d'investigation
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Intervention étudiée
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Type d'essai
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Plan de l'étude
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Critères d'inclusion/exclusion
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Critères d'évaluation principaux et secondaires
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Date d'enregistrement
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Inclusion du premier participant
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Sponsors secondaires
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Contacts supplémentaires
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ID secondaires
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Résultats-Données individuelles des participants
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Informations complémentaires sur l'essai
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Résultats de l'essai
Résumé des résultats
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Lien vers les résultats dans le registre primaire
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