Clinical trial · Observational
The Use of Indocyanine Green as a Diagnostic Adjunct for Pediatric Solid Malignancies
The Use of Indocyanine Green as a Diagnostic Adjunct for Pediatric Solid
- 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)
Use of indocyanine green will augment the accuracy of identification and resection of both primary solid malignancies as well as their pulmonary metastases, where applicable We will conduct a prospective feasibility study of pediatric patients with solid malignancies with or without lung metastatases who present at the time of initial diagnosis or relapse. These patients will receive a targeted dye to aid in the resection of these metastases. We plan to assess ICG as it relates to: 1. Diagnostic accuracy using pathologic correlation as gold standard measure 2. Short and long term event free and overall survival
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Metastatic Disease | — | UNRESOLVED | — |
| Primary Tumor | Primary Neoplasm | ALIAS | 0.90 |
| Solid Malignancies | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (2)
- measure
- Diagnostic accuracy using pathologic correlation as gold standard measure
- timeFrame
- 2 years
- measure
- Short and long term event free and overall survival
- timeFrame
- 2 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 1 Day
- Maximum age
- 45 Years
Show eligibility criteria text
Inclusion Criteria: All patients with newly diagnosed solid, primary malignancies or their related metastatic lesions. Diagnosis of primary or metastatic malignancy will be made by combination of: 1. Clinical evaluation and physical exam 2. Radiologic study including ultrasound, CT scan, and/or MRI 3. Pathologic diagnosis after biopsy Exclusion Criteria: 1. Those patients and parents/guardians unwilling to provide consent/assent. 2. Pregnant and/or women who are breast feeding. 3. Patients with Iodine allergies
References
Publications (0)
Data not yet available