Ireland
--:--IST
Recruiting Not applicable

Comparison of Biportal Versus Multiportal Robotic Approaches for Pulmonary Resection in NSCLC

NCT07818135 · tracked via the Priya Life Science Spain tracker
Sponsor
Carlos Déniz
Phase
Not applicable
Started
2026-01-15
Last updated
2026-09-14

Condition(s) studied

Non-Small Cell Lung Cancer

Investigational drug(s) / intervention(s)

Biportal Robotic-Assisted Thoracic SurgeryMultiportal Robotic-Assisted Thoracic Surgery

Biportal Robotic-Assisted Thoracic Surgery: Pulmonary resection performed with a biportal robotic-assisted thoracic surgery approach using two access incisions.

Multiportal Robotic-Assisted Thoracic Surgery: Pulmonary resection performed with a multiportal robotic-assisted thoracic surgery approach using multiple access ports.

Study summary

This study compares two established robotic surgical approaches for removing lung tumors in adults with non-small cell lung cancer: biportal robotic-assisted thoracic surgery (biRATS) and multiportal robotic-assisted thoracic surgery (multiRATS). Participants are assigned at random to one of the two approaches. The study will compare surgical safety, recovery after surgery, pain, length of hospital stay, quality of life, and other clinical outcomes during 12 months of follow-up.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 years or older, of any sex. * Non-small cell lung cancer considered clinically resectable, confirmed preoperatively or during surgery. * Candidate for pulmonary resection by robotic thoracic surgery. * Written informed consent. Exclusion Criteria: * Declines participation or cannot provide written informed consent. * Thoracic anatomical abnormalities that preclude or materially affect robotic surgery. * Active thoracic infection. * Surgery not performed by a participating surgeon with comparable experience in biRATS and multiRATS.

Primary outcome measure(s)

  • Incidence of Intraoperative and Immediate Postoperative Complications — From surgery through hospital discharge, up to 30 days
    Proportion of participants with intraoperative or immediate postoperative complications, classified by Clavien-Dindo grade. Events include, among others, prolonged air leak, pleuropulmonary infection, pneumothorax, postoperative hemorrhage, chylothorax, respiratory failure, wound infection, readmission, and perioperative death.

Trial sites (1)

FacilityCityRegionStatus
Hospital Universitari de Bellvitge L'Hospitalet de Llobregat Barcelona Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07818135 on ClinicalTrials.gov ↗ ← All trials in Spain