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NCT06903429: LUCAS

Using LUminoMark vs Coventional Practice for Targeted Axillary Surgery

Not yet recruiting NA Last updated 30 March 2025
What this trial tests

NA trial testing Targeting of axillary lymph nodes using LuminoMark in Breast Cancer in 330 participants. Not yet recruiting.

Timeline
1 May 2025
Primary endpoint
31 December 2026
31 December 2027

Quick facts

Lead sponsorKyungpook National University Chilgok Hospital
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment330
Start date1 May 2025
Primary completion31 December 2026
Estimated completion31 December 2027

Drugs / interventions tested

Conditions studied

Sponsor

Kyungpook National University Chilgok Hospital

Who can join

Adults 20 to 70, any sex, with Breast Cancer or Axillary Lymph Nodes. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study was to compare the use of LuminoMarkTM as a method of targeting axillary lymph nodes with other existing methods used in each institution, such as charcoal staining, needle targeting, and ultrasound-guided skin marking, in patients with breast cancer clinically suspected of metastasis, with or without clipping at the time of diagnosis, regardless of the presence or absence of neoadjuvant chemotherapy. By doing so, the investigators aimed to confirm the safety and usefulness of LuminoMarkTM as a targeting method.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Breast Cancer

Currently open trials in the same condition.

Other Kyungpook National University Chilgok Hospital trials

Trials by the same sponsor.

Verify against primary sources

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/NCT06903429.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing