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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04663191
Other study ID # T38
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2, 2020
Est. completion date December 3, 2020

Study information

Verified date December 2020
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Anatomical resection with systematic lymph-node dissection is currently the standard of care for the treatment of early stage non-small cell lung cancer. The use of minimally invasive approaches has increased greatly over the last two decades [either video-assisted thoracoscopic surgery (VATS) or robotic-assisted thoracoscopic surgery (RATS)], as they provide the patient with better outcomes than open thoracotomy. Minimally invasive VATS lobectomy for a standard case is generally a straightforward procedure for a well-trained surgical team, although concomitant preoperative pathologies or intraoperative findings/adverse events may result in technical difficulties, leading to intraoperative conversion, commonly by thoracotomy. The investigators aimed to assess long-term outcomes in a consecutive cohort of patients treated by anatomical pulmonary resection either using VATS, VATS requiring intraoperative conversion to thoracotomy, or upfront open thoracotomy for lung-cancer surgery.


Recruitment information / eligibility

Status Completed
Enrollment 843
Est. completion date December 3, 2020
Est. primary completion date December 2, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All consecutive patients treated by anatomical lobar pulmonary resection (lobectomy, bilobectomy) or anatomical sublobar pulmonary resection (segmentectomy) for non-small cell lung cancer (NSCLC), either by VATS (eventually with intraoperative conversion) or upfront thoracotomy. Exclusion Criteria: - patients with non-anatomical pulmonary resection (wedge resection) - patients with a histology other than NSCLC (benign or metastatic from another primitive cancer), stage IV NSCLC disease, - patients with multiple primary NSCLC (synchronous or metachronous) - patients with incomplete resection (R+) - patient for whom a VATS approach was never considered

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
anatomical resection
Anatomical resection with systematic lymph-node dissection

Locations

Country Name City State
France CHU Amiens Amiens

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival during the follow-up period after surgery from day of surgery up to 7 years
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