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Not Yet RecruitingNCT05038098

Magnetic Sentinel Lymph Node Mapping in Gastric Cancer

Magnetic Sentinel Lymph Node Mapping in Gastric Cancer, Safety and Feasibility Clinical Trial

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
M.D. Anderson Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This phase I finds out the possible benefits and/or side effects of using magnetic tracer FerroTrace and the fluorescent dye indocyanine green to identify the lymph nodes that cancer is most likely to have spread to in patients with gastric cancer that are undergoing gastrectomy. Using FerroTrace in combination with the indocyanine green dye may help researchers better detect the disease.

Detailed description

PRIMARY OBJECTIVE: I. To assess safety by assessing short term toxicity associated with the gastric injection of the novel magnetic tracer. SECONDARY OBJECTIVES: I. To determine the feasibility of sentinel lymph node (SLN) imaging and mapping using novel magnetic nanoparticles (iron conjugated polymers in saline suspension \[FerroTrace\]) for gastric cancer, and to determine whether pre-operative injection, intra-operative injection, or both are feasible. II. To test the validity of this procedure by correlating sentinel lymph nodes (SLN) to predict pathologic Lymph node (LN)-positive status i.e., will a negative SLN accurately predict the negativity of the other LNs? III. To determine the diagnostic value of additional hematoxylin and eosin (H\&E) sections and immunohistochemistry to assess sentinel lymph nodes compared to routine assessment with one H\&E stain alone. OUTLINE: Patients are assigned to 1 of 2 cohorts. COHORT I (PREOPERATIVE INJECTION): Patients receive FerroTrace peritumorally within days 1-21. Patients then undergo gastrectomy and receive indocyanine green (ICG) peritumorally. COHORT II (INTRAOPERATIVE INJECTION): Patients undergo gastrectomy and receive FerroTrace and ICG peritumorally during surgery.

Conditions

Interventions

TypeNameDescription
PROCEDUREGastrectomyUndergo surgery
DRUGIndocyanine GreenGiven peritumorally
OTHERIron Conjugated Polymers in Saline SuspensionGiven peritumorally

Timeline

Start date
2026-03-31
Primary completion
2027-02-02
Completion
2027-02-02
First posted
2021-09-08
Last updated
2026-03-05

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05038098. Inclusion in this directory is not an endorsement.