Skip to content

Ideal Marker for Targeted Axillary Dissection

Ideal Marker for Targeted Axillary Dissection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04580251
Acronym
IMTAD
Enrollment
100
Registered
2020-10-08
Start date
2021-01-01
Completion date
2023-05-30
Last updated
2023-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

breast cancer, axillary dissection, Magseed marker, iodine seed, carbon suspension, axillary lymph node

Brief summary

A multicentre prospective comparative study, comparing the use of various markers (magnetic marker Magseed, iodine seed 125I, carbon suspension) for marking a pathological lymph node in patients with breast carcinoma prior to neoadjuvant therapy and subsequent surgical treatment consisting of targeted axillary dissection.

Detailed description

There are two basic aims of the study 1. Prospective comparison of the reliability and accuracy of individual markers used for marking of a pathological axillary lymph node with subsequent targeted axillary dissection. 2. Comparison of the number of complications during localizing and detection of individual markers and postoperative complications. In individual collaborating centers, these markers are commonly used in clinical practice for marking of a pathological lymph node in patients with breast carcinoma. The usual standard of practice and treatment will not be changed in any way; the patients will only be prospectively followed. The study will bring an answer to the question of which marker is the best for marking lymph nodes. Apart from the basic demographic and other data (patient age, side of the body, size and characteristics of the tumor (typing, grading, staging), type and time of surgery, the incidence of complications during implantation or detection of the marker, number of lymph nodes, complications after surgery, and the final histological findings, also the following outcome measures will be observed: * depth of marker implantation (measured in mm) * marker migration (measured in mm) * success-rate of resection of the marked lymph node - assessment, whether the lymph node was removed (yes/no) using the respective marker, expressed in percent of successful removal for the respective marker * time from localizing the pathological lymph node using the marker to surgery (measured n days)

Interventions

The surgical treatment procedure of targeted axillary dissection performed in patients in whom the pathological lymph nodes have been marked using the examined and compared markers (magnetic marker Magseed, iodine seed 125I, carbon suspension)

Sponsors

Silesian Hospital in Opava
CollaboratorOTHER
Masaryk Memorial Cancer Institute
CollaboratorOTHER
EUC Clinic in Zlín
CollaboratorUNKNOWN
Institute for the Care of Mother and Child, Prague, Czech Republic
CollaboratorOTHER
University of Ostrava
CollaboratorOTHER
University Hospital Ostrava
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnosis of breast cancer, confirmed with a biopsy * indication of neoadjuvant therapy * biopsy of pathologically enlarged axillary lymph node and marking of the lymph node using one of the markers before neoadjuvant chemotherapy * surgical treatment after neoadjuvant chemotherapy (targeted axillary dissection)

Exclusion criteria

* refusal to participate in the study * another treatment protocol, which does not include targeted axillary dissection

Design outcomes

Primary

MeasureTime frameDescription
Depth of marker implantationDuring surgery/interventionThe depth of marker implantation will be assessed and measured in millimetres
Marker migrationDuring surgery/interventionMarker migration will be assessed and measured in millimetres
Success-rate of resection of the marked lymph node1 monthAssessment, whether the lymph node was removed (yes/no) using the respective marker, expressed in percent of successful removal for the respective marker.
Time from localizing the pathological lymph node using the marker to surgery1 monthThe time from localizing the pathological lymph node using the marker to surgery will be analysed and measured in days

Countries

Czechia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026