Home › Lung Cancer › NCT06252129
Maximizing Lymph Node Dissection on Fresh and Fixed Lung Cancer Resection Specimens
Who can join
Ages 18 and older · All sexes · Healthy volunteers welcome
Full eligibility criteria
Inclusion Criteria: 1. Subjects with a lung nodule or mass who are eligible to undergo a lobectomy. 2. Subject without any metastasis present. 3. Subjects who have peripheral lung nodule location 4. Subjects must be 18 years of age or older. Exclusion Criteria: 1. Subjects who received preoperative chemotherapy or radiotherapy. 2. Subjects who have a lung nodule located in a central location. Central tumors are defined by those infiltrating the lobar airway.
About the study
Lung cancer patients undergoing upfront surgery, highly benefit from a systematic lymph node dissection in the mediastinum and in the surgical specimens. The latter is performed by the pathologist. Developing a standardized technique to dissect the lobectomy specimen has the potential of maximizing the retrieval of all N1 stations lymph nodes. The investigators believe that the adoption of such technique will improve lung cancer staging and identify a higher number of patients that qualify for adjuvant therapies.
What is being tested
- Subjects undergoing a lung specimen lymph node dissection (other)
- Control group (other)
Sponsor: Brigham and Women's Hospital · Participants: 160 · Started: Jul 26, 2024
Contact the study team
- Paula Ugalde Figueroa, M.D. · Phone: (617) 732-7696
Official record on ClinicalTrials.gov — NCT06252129
Locations in the U.S.
| Massachusetts | Brigham and Womens Hospital, Boston |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.