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Completed

NCT Number: NCT02456649

Study of the Outcomes of Intraoperative Margin Assessment With MarginProbe

The combination of breast conserving surgery (lumpectomy) with radiation therapy has been shown to result in equivalent overall survival rates compared to mastectomy for the local treatment of breast cancer. As a result, the majority of patients diagnosed with breast cancer in the United States undergo lumpectomy as their primary surgical therapy. Multiple studies have demonstrated the association between positive lumpectomy margins and an increased risk of ipsilateral breast tumor recurrence, even with postoperative radiation. Studies report 20-40% of lumpectomy procedures result in one or more involved (positive) surgical margins, leading to the need for further surgery, emotional distress, poorer cosmesis, delay to adjuvant treatments, and increased cost. Current available intraoperative margin assessment techniques include specimen Xray, gross pathology, frozen section, and touch prep cytology. To reduce the incidence of positive margins, the MarginProbe (Dune Medical Devices, Caesarea, Israel) was developed to provide real-time, intraoperative assessment of the presence of tumor at the lumpectomy margin. In the current study, the investigators aim to determine the effectiveness of MarginProbe as an adjunctive tool to standard practice for intraoperative identification of tumor at lumpectomy margins, and its ability to reduce positive margins and decrease the need for additional surgical procedures.

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Huntington Memorial Hospital

Pasadena, California, 91105, United States

About this study

In the current study, the investigators aim to determine the effectiveness of MarginProbe as an adjunctive tool to standard practice for intraoperative identification of tumor at lumpectomy margins, and its ability to reduce positive margins and decrease the need for additional surgical procedures.

Aims of the study:

Primary objectives

  • Determine positive margin rate following lumpectomy

Secondary objectives

  • Determine accuracy of intraoperative margin assessment with use of MarginProbe plus standard of care (gross pathologic examination and/or intraoperative specimen Xray) versus standard of care (gross pathologic examination and/or intraoperative specimen Xray) alone.
  • Determine impact of MarginProbe on total tissue volume removed
  • Determine the impact of MarginProbe on the need for additional surgical procedures.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects able to read and understand the informed consent

Exclusion criteria

  • Subjects unable to read or understand the informed consent.

Treatment and study plan

MarginProbe

Device

Intraoperative MarginProbe use as adjunct to standard practice MarginProbe will be used on the lumpectomy specimen within 20 minutes of excision, prior to specimen Xray or gross pathology evaluation. This may take up to 5 minutes. MarginProbe will indicate a positive or negative reading for each of the 6 circumferential margins, and the results will be recorded. Any margins determined by to < 5-10 mm by specimen Xray or gross pathology examination will be re-excised. In addition, any additional margins not already identified as < 5-10 mm, but identified as positive by MarginProbe will be re-excised where feasible.

Primary outcomes

  1. Percentage of patients with histologically positive surgical margins

    Time frame: 2 weeks after surgery

Secondary outcomes

  1. Percentage of patients who undergo a second surgery after initial lumpectomy.

    Time frame: 2 weeks after surgery

  2. False positive and false negative rate of Intraop MarginProbe results compared to histologic evaluation

    Time frame: 2 weeks after surgery

Sponsors and collaborators

Lead sponsor

Huntington Memorial Hospital

Other

Registry information

Official study title

A Phase II Study of the Outcomes of Intraoperative Margin Assessment With Adjunctive Use of MarginProbe in Addition to Standard

Acronym: MarginProbe

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
May 28, 2015
Registry last updated
Oct 4, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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