search
Back to results

Sentinel Lymph Node Mapping Using Magtrace and MRI in Healthy Subjects for Potential Use in Melanoma Patients (TRACIE)

Primary Purpose

Melanoma

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Sentinel node mapping using MRI
Sponsored by
Zuyderland Medisch Centrum
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Melanoma focused on measuring Magnetic tracer, Sentinel lymph node, Melanoma, MRI

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy participants;
  • Participants should be ≥18 years of age at the time of consent;
  • Participants should be willing to provide informed consent.

Exclusion Criteria:

  • Known intolerance/hypersensitivity to iron, dextran compounds or Magtrace® itself;
  • Standard MRI exclusion criteria:
  • Implantable (electrical) devices (e.g. pacemaker, cochlear implants, neurostimulator);
  • Any other metal implants;
  • Claustrophobia;
  • MR-incompatible prosthetic heart valves;
  • Tattoos inked with metallic dye.
  • Participants who refuse to provide informed consent.

Sites / Locations

  • Zuyderland Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Healthy participants

Arm Description

Outcomes

Primary Outcome Measures

SPIO dosage in milliliters
SPIO dosage in milliliters will be assessed to develop a pre-operative MRI protocol. Testing will be perform in healthy subjects.
Massage duration in seconds
Massage duration in seconds will be assessed to develop a pre-operative MRI protocol. Testing will be perform in healthy subjects.
Time to artefact appearance in minutes
Time to artefact appearance in minutes will be assessed to develop a pre-operative MRI protocol. Testing will be perform in healthy subjects.

Secondary Outcome Measures

Full Information

First Posted
September 9, 2021
Last Updated
September 5, 2022
Sponsor
Zuyderland Medisch Centrum
search

1. Study Identification

Unique Protocol Identification Number
NCT05054062
Brief Title
Sentinel Lymph Node Mapping Using Magtrace and MRI in Healthy Subjects for Potential Use in Melanoma Patients
Acronym
TRACIE
Official Title
Sentinel Lymph Node Mapping With Superparamagnetic Iron Oxide for Melanoma: a Pilot Study in Healthy Participants to Establish an Optimal MRI Workflow Protocol
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
August 20, 2021 (Actual)
Study Completion Date
August 20, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zuyderland Medisch Centrum

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Sentinel lymph node biopsy (SLNB) is crucial in the management of malignant melanoma treatment and is currently performed by pre-operatively inject a colloid nanomaterial labeled with Technetium (99mTc) as radioactive tracer. Intra-operatively, Patent Blue (PB) will be injected to improve the visualization of the lymphatic tract. However, current pre-operative SLN mapping technique, is associated with disadvantages as radiation exposure for both patients and health care personnel and logistic challenges, because of time constraints due to short half-live time of 99mTc. Superparamagnetic iron oxide (SPIO) is novel, non-radioactive technique using a magnetic tracer (Magtrace® (Endomagnetics Ltd.)) and several studies showed that SPIO is non-inferior to dual tracing with 99mTc and PB in breast cancer patients. SPIO is expected to be non-inferior to dual tracing with 99mTc and PB in melanoma patients. However, further research is needed to demonstrate the use of SPIO in pre-operative Magnetic Resonance Imaging (MRI) scanning. Guidance on pre-operative MRI use is rather limited, though fundamental in the intended research process. Hence, the aim of this subprotocol study, which includes healthy subjects, is to develop a pre-operative MRI protocol for melanoma patients. The acquired knowledge will be used to design a feasibility study, including a larger group of melanoma patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma
Keywords
Magnetic tracer, Sentinel lymph node, Melanoma, MRI

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
6 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Healthy participants
Arm Type
Experimental
Intervention Type
Diagnostic Test
Intervention Name(s)
Sentinel node mapping using MRI
Intervention Description
Sentinel lymph node mapping in melanoma patients using a magnetic tracer and MRI
Primary Outcome Measure Information:
Title
SPIO dosage in milliliters
Description
SPIO dosage in milliliters will be assessed to develop a pre-operative MRI protocol. Testing will be perform in healthy subjects.
Time Frame
Three weeks
Title
Massage duration in seconds
Description
Massage duration in seconds will be assessed to develop a pre-operative MRI protocol. Testing will be perform in healthy subjects.
Time Frame
Three weeks
Title
Time to artefact appearance in minutes
Description
Time to artefact appearance in minutes will be assessed to develop a pre-operative MRI protocol. Testing will be perform in healthy subjects.
Time Frame
Three weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy participants; Participants should be ≥18 years of age at the time of consent; Participants should be willing to provide informed consent. Exclusion Criteria: Known intolerance/hypersensitivity to iron, dextran compounds or Magtrace® itself; Standard MRI exclusion criteria: Implantable (electrical) devices (e.g. pacemaker, cochlear implants, neurostimulator); Any other metal implants; Claustrophobia; MR-incompatible prosthetic heart valves; Tattoos inked with metallic dye. Participants who refuse to provide informed consent.
Facility Information:
Facility Name
Zuyderland Medical Center
City
Sittard
State/Province
Limburg
ZIP/Postal Code
6162BG
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36241982
Citation
Aldenhoven L, Frotscher C, Korver-Steeman R, Martens MH, Kuburic D, Janssen A, Beets GL, van Bastelaar J. Sentinel lymph node mapping with superparamagnetic iron oxide for melanoma: a pilot study in healthy participants to establish an optimal MRI workflow protocol. BMC Cancer. 2022 Oct 14;22(1):1062. doi: 10.1186/s12885-022-10146-w.
Results Reference
derived

Learn more about this trial

Sentinel Lymph Node Mapping Using Magtrace and MRI in Healthy Subjects for Potential Use in Melanoma Patients

We'll reach out to this number within 24 hrs