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Recruiting NCT07818135

NCT07818135 Comparison of Biportal Versus Multiportal Robotic Approaches for Pulmonary Resection in NSCLC

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Clinical Trial Summary
NCT ID NCT07818135
Status Recruiting
Phase —
Sponsor Carlos Déniz
Condition Non-Small Cell Lung Cancer
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2026-01-15
Primary Completion 2028-02

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Biportal Robotic-Assisted Thoracic SurgeryMultiportal Robotic-Assisted Thoracic Surgery

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 80 participants in total. It began in 2026-01-15 with a primary completion date of 2028-02.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

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.

Contact & Investigator

Central Contact

Carlos Déniz Armengol, MD, PhD

✉ cjdeniz@bellvitgehospital.cat

📞 +34 932607500

Principal Investigator

Carlos Déniz Armengol, MD, PhD

PRINCIPAL INVESTIGATOR

Hospital Universitari de Bellvitge

Frequently Asked Questions

Who can join the NCT07818135 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Non-Small Cell Lung Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07818135 currently recruiting?

Yes, NCT07818135 is actively recruiting participants. Contact the research team at cjdeniz@bellvitgehospital.cat for enrollment information.

Where is the NCT07818135 trial being conducted?

This trial is being conducted at L'Hospitalet de Llobregat, Spain.

Who is sponsoring the NCT07818135 clinical trial?

NCT07818135 is sponsored by Carlos Déniz. The principal investigator is Carlos Déniz Armengol, MD, PhD at Hospital Universitari de Bellvitge. The trial plans to enroll 80 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology