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Recruiting NCT07790406

NCT07790406 Surgical Outcome Of da Vinci Single-port Surgical System In Lung Cancer

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Clinical Trial Summary
NCT ID NCT07790406
Status Recruiting
Phase —
Sponsor European Institute of Oncology
Condition Lung Cancer (NSCLC)
Study Type OBSERVATIONAL
Enrollment 50 participants
Start Date 2026-02-02
Primary Completion 2032-03

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
da Vinci Single Port

Eligibility Fast-Check

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

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 50 participants in total. It began in 2026-02-02 with a primary completion date of 2032-03.

⚠ 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

Early-stage lung cancer represents a clinical challenge that, when diagnosed promptly, offers high chances of cure through lobectomy and lymphadenectomy. In addition to traditional surgery, robotic techniques have become established and have recently evolved further with the Single-Port system, which allows the procedure to be performed through a single subcostal incision rather than multiple openings between the ribs. This approach reduces invasiveness, postoperative pain, and recovery time, while maintaining the same oncological effectiveness and safety as standard techniques. This is a monocentric and non-profit collection of clinical data, both prospective and retrospective, from patients treated with this method, ensuring data privacy through coded information and compliance with current regulations; the study is independent and non-profit.

Eligibility Criteria

Inclusion Criteria: * all patients with proven non-small cell lung cancer (NSCLC) clinical stage I (9th TNM edition), who have undergone or will undergo lobectomy plus radical lymph node dissection following the STS guide line Exclusion Criteria: * no consent

Contact & Investigator

Central Contact

Monica Casiraghi, MD PhD

✉ monica.casiraghi@ieo.it

📞 025748662

Frequently Asked Questions

Who can join the NCT07790406 clinical trial?

This trial is open to participants of all sexes, studying Lung Cancer (NSCLC). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07790406 currently recruiting?

Yes, NCT07790406 is actively recruiting participants. Contact the research team at monica.casiraghi@ieo.it for enrollment information.

Where is the NCT07790406 trial being conducted?

This trial is being conducted at Milan, Italy.

Who is sponsoring the NCT07790406 clinical trial?

NCT07790406 is sponsored by European Institute of Oncology. The trial plans to enroll 50 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