Minimally invasive segmentectomy versus lobectomy for stage I lung cancer: recovery and quality of life

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational study collecting patient-reported outcomes before surgery and at multiple points during the first year after minimally invasive segmentectomy or lobectomy for stage I NSCLC. Participants complete questionnaires on dyspnea, physical function, and health-related quality of life, and outcomes after video-assisted (VATS) versus robotic-assisted (RATS) approaches are compared. Patients with recent thoracic surgery, neoadjuvant therapy, or who fail to complete baseline questionnaires are excluded. The study is conducted at Hospital Universitario Ramón y Cajal in Madrid and uses routine surgical care rather than experimental interventions.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients with clinical stage I NSCLC who undergo segmentectomy or lobectomy with VATS or RATS.

Exclusion Criteria:

* Thoracic surgery in the previous year
* Neoadyuvant treatment
* Failure to complete preoperative questionnaires

Where it's running

• Hospital Universitario Ramón y Cajal
  Madrid, Madrid, Spain Recruiting

Study contacts

• Principal investigator: Sara Fra, MD — Hospital Universitario Ramon y Cajal
• Study coordinator: Sara Fra, MD
• Email: sarafrafernandez@gmail.com
• Phone: 0034913369102

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.