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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05569707
Other study ID # NL79537.100.21
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 2023
Est. completion date March 2024

Study information

Verified date October 2022
Source University of Twente
Contact Anke Christenhusz, MSc
Phone +3153 489 1592
Email a.christenhusz@utwente.nl
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date March 2024
Est. primary completion date January 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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: - 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.)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Magnetic 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®).

Locations

Country Name City State
Netherlands Medisch Spectrum Twente Enschede
Netherlands Ziekenhuisgroep Twente (ZGT) Hengelo

Sponsors (1)

Lead Sponsor Collaborator
University of Twente

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 (MagtraceĀ®) and hand-held magnetometer DiffMag. through study completion, an average of 1 year
Primary 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 (MagtraceĀ®) and hand-held magnetometer Sentimag. through study completion, an average of 1 year
Secondary 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. through study completion, an average of 1 year
Secondary 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. through study completion, an average of 1 year
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