Clinical trial · Interventional
Non-invasive Fluorescent Imaging System for Imaging Mohs Tumor
Near Infra-Red Navigation (NAVI) System for Mohs Tumor Mapping
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The objective of this study is to correlate traditional histological Mohs tissue mapping of a cutaneous tumor with the ICG-mapping procedure. The use of intradermal ICG in a cutaneous tumor during MMS followed by visualization using a fluorescent imaging system could allow surgeons to directly visualize, and roughly map the extent of a primary skin cancer and plan the Mohs procedure (i.e. the initial excision size and subsequent layer widths) accordingly.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Skin Cancer | Malignant Skin Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| NAVI mapping with Indocyanine green | Combination Product | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- NAVI mapping with Indocyanine green
- description
- Participants will undergo their scheduled Mohs surgery with the addition of the NAVI mapping with ICG dye
- interventionNames
- Combination Product: NAVI mapping with Indocyanine green
Primary outcomes (1)
- measure
- Near Infra-Red Navigation (NAVI) System for Mohs Tumor Mapping
- timeFrame
- 24 HOURS
- description
- Correlation of traditional histological Mohs tissue mapping of a cutaneous tumor with the ICG-mapping procedure.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: Subjects who are scheduled to undergo Mohs surgery for a basal cell carcinoma tumor, with a minimum tumor size of 1.5 cm, will be selected for the study procedure. A total of 10 subjects are required to complete the study. We will need to consent 15 subjects to achieve a total of 10 subjects to complete the study. * Individuals 18 years or older * All races and ethnicity * Smokers and non-smokers Exclusion Criteria: \-
References
Publications (0)
Data not yet available