Clinical trial · Interventional
Evaluation of a Novel Axillary Lymph Node Ink Localization Technique: A Feasibility Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): The study was never activated / began due to hospital staff and resources being re-allocated to support the demands of the Covid-19 global pandemic.
Summary
Brief summary (as posted)
Patients with breast cancer and metastatic axillary lymphadenopathy routinely undergo neo-adjuvant chemotherapy. For these patients, biopsy clip markers are inserted into the biopsy proven metastatic lymph node pre-treatment, as they may reach complete clinical response post-therapy. Limited axillary surgery, as opposed to a full axillary dissection, may then be indicated. It is still necessary to surgically excise the biopsy proven metastatic lymph node to accurately assess the pathologic response to therapy, and subsequently tailor post-surgical therapies appropriately. As such, these lymph nodes require pre-operative localization which, at The Ottawa Hospital, currently requires radioactive seed insertion under sonographic guidance, typically performed within 5 days of surgery. The procedure is often challenging, as both normal appearing lymph nodes and 3 mm biopsy clip markers are difficult and in some cases impossible, to visualize on ultrasound. At the time of surgery, the excised lymph node is radiographed, to ensure the radioactive seed and biopsy clip marker are both successfully excised. Localization with Ink has the potential to replace both the biopsy clip markers and radioactive seeds as the surgeons are able to directly visualize the Ink intra-operatively and excise the Inked lymph node. A preliminary study out of Stanford on 28 patients who underwent localization of axillary lymph nodes with Ink injected 1-211 days pre-operatively, in the pre neo-adjuvant and post neo-adjuvant settings, showed that lymph nodes injected with Ink are visible intra-operatively months after surgery, suggesting that this is a feasible localization technique (1).
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Axillary Lymphadenitis | — | UNRESOLVED | — |
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Black-Eye Ink | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Ink placed before chemotherapy (Study A)
- description
- In Study A, 0.5 mL of Black Eye Ink will be placed in the metastatic LN after neoadjuvant therapy
- interventionNames
- Device: Black-Eye Ink
- type
- ACTIVE_COMPARATOR
- label
- Ink placed after chemotherapy (Study B)
- description
- In Study B, 0.5 mL of Black Eye Ink will be placed before neoadjuvant therapy
- interventionNames
- Device: Black-Eye Ink
Primary outcomes (4)
- measure
- Identification rate of Inked nodes, containing seed and clip
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * English or French speaking female patients, with a personal history of current pathologically proven breast cancer, over the age of 18 years \[patients \<18 would be considered a rare occurrence\] * Patients who will be undergoing neoadjuvant chemotherapy * Patients who will be undergoing axillary lymph node radioactive seed localization * Patients who will be undergoing axillary surgery Exclusion Criteria: * Allergic reaction to Black Eye Ink or any of its components * Pregnancy * Confirmed metastatic disease
References
Publications (0)
Data not yet available