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Status unknownNCT05569707MelaDiffUpdated Oct 6, 2022

MR Lymphography and Magnetic Sentinel Lymph Node Biopsy in Melanoma Patients

An interventional study of Magnetic sentinel lymph node biopsy by use of Magtrace®, in combination with SentiMag® and DiffMag in Melanoma (Skin), sponsored by University of Twente. Status unknown at 2 sites in Netherlands. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-10-06.

Sponsored by University of Twente · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Oct 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The sentinel lymph nodes (SLNs) are the first lymph nodes (LNs) to drain the tumor site and therefore the first LNs to bare metastases. Hence the importance to investigate these LNs for the best treatment strategy. Current-standard-of-care for melanoma patients with a melanoma stage of pT1b or higher, involve a surgical procedure, referred to as SLN biopsy (SLNB). The SLNB procedure involves a combined detection procedure using a radio-active tracer and blue dye followed by surgical dissection and evaluation of the LNs at the histopathology department. Due to the use of radioisotopes, this procedure suffers from several disadvantages such as limited availability, strict rules and regulations, degradation time in patient and radioactive load for user and patient.

To overcome the limitations of a radioactive tracer, a magnetic SLNB was developed which is facilitated by super paramagnetic iron-oxide (SPIO) nanoparticles. This potentially offers numerous benefits making surgery planning more flexible: no exposure to radiation, easy accessibility of the tracer, long shelf life and long half time in the patient. However, the currently available magnetometer for intraoperative detection of SPIO-enhanced LNs is hampered by a relatively low detection depth, biological noise, and effects of surgical equipment. Therefore, surgeons need to switch to plastic or carbon equipment and the system needs to be balanced prior to each measurement, which increases the surgery time.

A new and effective way to localize SPIOs is differential magnetometry (DiffMag). This patented detection principle, developed by MD\&I group at University of Twente (UT), utilizes the nonlinear magnetic response of nanoparticles. An additional advantage of SPIOs is their visibility on MRI, which could provide mapping the SLNs preoperatively. Especially in patients with melanomas on the abdomen or back this would be very useful to see which lymph node stations are connected to the melanoma. In addition, studies have shown that SPIOs are absorbed into lymph nodes in different ways, depending on the presence of metastases. SPIO-enhanced MR lymphography could therefore provide an opportunity for a non-invasive preoperative assessment of nodal status.

In this pilot study the investigators want to evaluate the clinical use of the DiffMag handheld probe. Moreover, the investigators want to map the lymph nodes (metastases) preoperatively using MR lymphography.

02

Conditions studied

  • Melanoma (Skin)

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Keywords

  • Magnetic sentinel lymph node biopsy (SLNB)
  • Lymph node detection
  • Lymph node staging
  • MR lymphography
  • Super paramagnetic iron-oxide (SPIO) nanoparticles
03

In context

Melanoma

3,006 studies on the registry are indexed under Melanoma; 520 are open to participants now.

This study's planned enrollment of 20 is below the median of 38 across 2,351 interventional studies indexed under Melanoma.

Browse Melanoma studies →

Lead sponsor

University of Twente is the lead sponsor of 16 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with melanoma of the upper or lower extremities scheduled for SLNB;
  • Willing to \& able to write informed consent from the subject prior to participation;
  • Willing to \& capable of following study procedures;
  • Is older than 18 years;
  • Speaks and understand the Dutch language

Exclusion criteria

Exclusion Criteria:

  • Intolerance / hypersensitivity to iron or dextran compounds
  • Pregnant or lactating patients;
  • Patients having a pacemaker.
  • Patients non eligible for MRI investigation (pacemakers or other implantable devices in the chest wall and/or lower body, claustrophobic, etc.)
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Other
    MelaDiff

    Patients with melanoma of the extremities included in the protocol. Preoperative, patients will receive two MRI-scans and a magnetic tracer injection at the primary tumor site. During surgery, SLNs will be detected using two types of magnetometers (SentiMag® \& DiffMag) in combination with Magtrace®, in addition to the standard procedure.

    Device: Magnetic sentinel lymph node biopsy by use of Magtrace®, in combination with SentiMag® and DiffMag

Interventions

  • DeviceMagnetic sentinel lymph node biopsy by use of Magtrace®, in combination with SentiMag® and DiffMag

    In addition to the standard procedure, SLNs will be detected using two types of magnetometers (SentiMag® \& DiffMag) in combination with SPIO particles (Magtrace®).

06

What researchers measure

Primary outcomes

  1. True positive/False negative rate for a magnetic SLN detection measured by DiffMag system compared to radioactive detection.

    Determining the feasibility of SLN detection/localization in melanoma patients using a magnetic tracer (Magtrace®) and hand-held magnetometer DiffMag.

    Time frame: through study completion, an average of 1 year

  2. True positive/False negative rate for a magnetic SLN detection measured by Sentimag system compared to radioactive detection.

    Determining the feasibility of SLN detection/localization in melanoma patients using a magnetic tracer (Magtrace®) and hand-held magnetometer Sentimag.

    Time frame: through study completion, an average of 1 year

Secondary outcomes

  1. True positive/False negative rate for metastatic SLN using ex vivo MRI

    Determining the feasibility of LN mapping with preoperative SPIO-enhanced MR lymphography and examining the use of SPIO-enhanced MR lymphography for LN staging.

    Time frame: through study completion, an average of 1 year

  2. True positive/False negative rate for metastatic SLN using in vivo MRI

    Determining the feasibility of LN mapping with preoperative SPIO-enhanced MR lymphography and examining the use of SPIO-enhanced MR lymphography for LN staging.

    Time frame: through study completion, an average of 1 year

07

Study locations

2 sites
  • Medisch Spectrum Twente
    Enschede, Netherlands
    • Anneriet Dassen · Principal investigator
  • Ziekenhuisgroep Twente (ZGT)
    Hengelo, Netherlands
    • Daniëlle de Leeuw · Principal investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 6, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05569707
Lead sponsor
University of Twente
Responsible party
Anke Christenhusz (PhD student / coordinating investigator, University of Twente) — Principal investigator
First posted
Oct 6, 2022
Start date
Jan 2023 (estimated)
Primary completion
Jan 2024 (estimated)
Completion
Mar 2024 (estimated)
Last update
Oct 6, 2022

Study contacts

Anke Christenhusz, MSc
Contact
a.christenhusz@utwente.nl
+3153 489 1592
Lejla Alic, PhD
Contact
l.alic@utwente.nl
+3153 489 1592
Lejla Alic, PhD
study chair · University of Twente
Anneriet Dassen, PhD
principal investigator · Medisch Spectrum Twente Enschede

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.

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