Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06383663

Supraclavicular Lymph Node Dissection for Ipsilateral Supraclavicular Lymph Node Metastatic Breast Cancer

A Prospective Multicenter Randomized Controlled Trial of the Prognostic Effects of Supraclavicular Lymph Node Dissection vs. No-dissection in Ipsilateral Supraclavicular Lymph Node Metastasis in Breast Cancer

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
452 (estimated)
Sponsor
Sun Yat-sen University · Academic / Other
Sex
Female
Age
35 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to compare the efficacy of surgical dissection of supraclavicular lymph nodes combined with radiotherapy versus radiotherapy alone in patients with ipsilateral supraclavicular lymph node metastasis.

Detailed description

In this study, patients with ipsilateral supraclavicular lymph node positive breast cancer were selected as research subjects. Randomized controlled method was used to study the effects of surgical dissection of supraclavicular lymph node combined with radiotherapy and radiotherapy alone on progression-free survival and overall survival of breast cancer. This RCT aims to explore the best treatment method for ipsilateral supraclavicular lymph node metastasis and to provide the basis for guiding the precise treatment of supraclavicular lymph node chain.

Conditions

Interventions

TypeNameDescription
PROCEDURESupraclavicular lymph node dissection combined with radiotherapyBreast cancer patients in the expreimental cohort with only ipsilateral supraclavicular lymph node metastasis were first treated with supraclavicular lymph node dissection and received standard radiotherapy after surgery.
RADIATIONradiotherapyPatients in the control group received only standard radiation therapy.

Timeline

Start date
2024-05-01
Primary completion
2028-12-31
Completion
2029-12-31
First posted
2024-04-25
Last updated
2024-04-30

Source: ClinicalTrials.gov record NCT06383663. Inclusion in this directory is not an endorsement.