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NCT06149377

Impact of a Predictive Model on Sentinel Lymph Node Biopsy in Initially Lymph Node-positive, HER2-positive Breast Cancer

Completed Last updated 13 December 2023
What this trial tests

trial testing Test cohort in Breast Cancer in 716 participants. Completed in 31 May 2023.

Timeline
1 April 2012
Primary endpoint
31 May 2023
31 May 2023

Quick facts

Lead sponsorFujian Medical University Union Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment716
Start date1 April 2012
Primary completion31 May 2023
Estimated completion31 May 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fujian Medical University Union Hospital

Who can join

Eligibility, female only, with Breast Cancer or Sentinel Lymph Node. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study was to develop and validate a nomogram to assess axillary pathological complete response (pCR) in patients with initially lymph node-positive, human epidermal growth factor receptor 2 (HER2)-positive breast cancer and test its performance in guiding patient selection for sentinel lymph node biopsy (SLNB) following neoadjuvant systemic therapy (NST).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Breast Cancer

Currently open trials in the same condition.

Other Fujian Medical University Union Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06149377.

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