Actively Recruiting

Age: 18Years +
All Genders
ID06470607

Biological Observational Monocentric Study Aimed at Analyzing the Lymphocytic Infiltrate of Lung Tumors

Led by Scientific Institute San Raffaele · Updated on 2024-11-29

70

Participants Needed

1

Research Sites

105 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a monocentric observational study to explore the molecular structure of tumors in the thoracic cavity, focusing on non-small cell lung cancer (NSCLC). The study aims to better understand the lymphocytic infiltrate within lung tumors by collecting clinical data and biological samples from patients diagnosed with thoracic tumors. Participants will be patients over 18 years old who are candidates for surgical treatment of thoracic tumors. During hospitalization and surgery, clinical data and biological material such as blood and tumor tissue will be collected. There is only one hospital visit for these procedures, and no follow-up data collection after discharge. The study is planned to last three years. During the single hospital visit, participants will undergo standard clinical procedures related to their treatment. Researchers will isolate lymphocytes within 15 days from enrollment to surgery and analyze lymphocyte gene expression within 48 hours after surgery. The study focuses on detailed biological analysis without further interventions, and participant observation is limited to the surgery period.

CONDITIONS

Brief Title

The Lymphocytic Infiltrate of Lung Tumors.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ability to provide informed consent
  • Men and women over the age of 18
  • Patients candidates for surgical treatment diagnosed with thoracic tumors
Not Eligible

You will not qualify if you...

  • Previous chemotherapy for any cancer within the last 6 months
  • Pregnant and/or breastfeeding women
  • Immunosuppressive state (states of immunosuppression or ongoing immunosuppressive/immunomodulatory treatments)

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 15 days

Participants undergo surgical treatment for thoracic tumors during hospitalization. Biological samples and data are collected during this single hospital visit as part of standard clinical care.

1 hospital visit (in-person)

Trial Site Locations

Total: 1 location

1

Scientific Institute Ospedale San Raffaele

Milan, Italy, 20132

Actively Recruiting

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Research Team

P

Pierluigi Novellis, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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