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NCT02910726

A Study Comparing Green Fluorescent Dye and Radioactive Dye for Sentinel Lymph Node Biopsy in Pediatric Cancers

Completed Phase 2, PHASE3 Results posted Last updated 5 October 2022
What this trial tests

Phase 2, PHASE3 trial testing Sentinel Lymph Node Biopsy in Pediatric Patients With Solid Tumors in 6 participants. Completed in 2 September 2022.

Timeline
13 September 2016
Primary endpoint
2 September 2022
2 September 2022

Quick facts

Lead sponsorMemorial Sloan Kettering Cancer Center
PhasePhase 2, PHASE3
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment6
Start date13 September 2016
Primary completion2 September 2022
Estimated completion2 September 2022
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Memorial Sloan Kettering Cancer Center — full company profile →

Who can join

Under 30, any sex, with Pediatric Patients With Solid Tumors. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is being done in patients that have tumors to find out how well sentinel lymph nodes (SLNs) can be found with a special dye called indocyanine green (ICG).

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 trials of Sentinel Lymph Node Biopsy

Trials testing the same drug.

Other Memorial Sloan Kettering Cancer Center 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/NCT02910726.

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