GeneSearch™ Breast Lymph Node (BLN) Assay China Registration Study

May 29, 2013 updated by: Johnson & Johnson Medical, China

一项比较GeneSearch 乳腺淋巴结(BLN)检测试剂盒和永久病理切片检测乳腺癌患者腋窝前哨淋巴结转移的前瞻性、多中心临床试验 A Prospective and Multi-center Clinical Trial By Comparing GeneSearch™ Breast Lymph Node (BLN) Test Kit To Permanent Pathological Section On Detecting Axillary Sentinel Lymph Node Metastases In Breast Cancer Patients

The primary objective of this trial is to compare GeneSearch™ Breast Lymph Node (BLN) Test Kit to permanent pathological section, so as to evaluate the clinical sensitivity and specificity of GeneSearch™ Breast Lymph Node (BLN) Test Kit in detecting axillary sentinel lymph node metastases in breast cancer patients.

The secondary objective of this trial is to evaluate the positive predictive value and negative predictive value of GeneSearch™ Breast Lymph Node (BLN) Test Kit when used in the detection of axillary sentinel lymph node metastases in breast cancer patients.

Prospective and multi-center clinical trial

Study Overview

Status

Terminated

Conditions

Study Type

Interventional

Enrollment (Actual)

540

Phase

  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Shanghai, China, 200032
        • Shanghai Cancer Hospital
    • Beijing
      • Beijing, Beijing, China, 100035
        • Beijing Cancer Hospital
    • Guangdong
      • Guangdong, Guangdong, China, 510080
        • Guangdong General Hospital
      • Guangzhou, Guangdong, China
        • Second Affiliated Hospital of Zhongshan University
    • Shandong
      • Jinan, Shandong, China, 250117
        • China Shandong Cancer hospital
    • Sichuan
      • Chongqing, Sichuan, China, 400038
        • Southwest Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Diagnosed previously as breast cancer
  • patient scheduled for sentinel lymph node dissection
  • 18 years or older
  • female or male, and
  • able and willing to give consent to participate in the study

Exclusion Criteria:

  • Patients taking part in other research studies that would interfere with their full participation in this study, or
  • Prior sentinel or partial axillary lymphadenectomy on the same body side

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Routine pathologic method
Half of each sentinal lymph node will have rountine pathologic examination as normal practice.
Experimental: GeneSearch BLN Assay
Half of each sentinal lymph node will have GeneSearch BLN testing.

Each of the sentinal lymph node will be divided in half according to cutting scheme.

Half of the sentinal lymph node will be tested using rountine pathological method as normal practice, half of the node will have GeneSearch BLN testing.

Other Names:
  • GeneSearch
  • Pathology

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
To compare GeneSearch™ BLN Test Kit to permanent pathological section to evaluate the clinical sensitivity and specificity of GeneSearch™ BLN Test Kit in detecting axillary sentinel lymph node metastases in breast cancer patients.
Time Frame: 9 months
9 months

Secondary Outcome Measures

Outcome Measure
Time Frame
To evaluate the positive predictive value and negative predictive value of GeneSearch™ BLN Test Kit when used in the detection of axillary sentinel lymph node metastases in breast cancer patients.
Time Frame: 9 months
9 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Yongsheng Wang, MD, Shandong Cancer Hospital and Institute

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 1, 2009

Primary Completion (Actual)

October 1, 2009

Study Completion (Actual)

November 1, 2009

Study Registration Dates

First Submitted

March 25, 2009

First Submitted That Met QC Criteria

March 25, 2009

First Posted (Estimate)

March 26, 2009

Study Record Updates

Last Update Posted (Estimate)

May 30, 2013

Last Update Submitted That Met QC Criteria

May 29, 2013

Last Verified

June 1, 2009

More Information

Terms related to this study

Other Study ID Numbers

  • OCD-200804
  • CBCSG-001a

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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