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Trial record 1 of 4 for:    novilase
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A Multicenter "Ablate and Resect" Study of Novilase® Interstitial Laser Therapy for the Ablation of Small Breast Cancers

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01478438
Recruitment Status : Unknown
Verified March 2021 by Novian Health Inc..
Recruitment status was:  Active, not recruiting
First Posted : November 23, 2011
Last Update Posted : March 3, 2021
Information provided by (Responsible Party):
Novian Health Inc.

Brief Summary:
This study will determine the rate of complete tumor ablation of small breast cancers (≤ 20mm) by Novilase Interstitial Laser Therapy (ILT), and determine the sensitivity and specificity of imaging (MRI, mammography and ultrasound) in detecting residual tumor post ILT ablation as correlated to histopathology from the post-ablation excision.

Condition or disease Intervention/treatment Phase
Malignant Tumor Device: Novilase Interstitial Laser Therapy Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 60 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Multicenter "Ablate and Resect" Study of Novilase® Interstitial Laser Therapy for the Ablation of Small Breast Cancers
Study Start Date : April 2012
Actual Primary Completion Date : December 2015
Estimated Study Completion Date : August 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer

Arm Intervention/treatment
Experimental: Treat and Excise
All subjects will be treated with Interstitial Laser Therapy (ILT) followed by excision no later than 28 days post ablation.
Device: Novilase Interstitial Laser Therapy
Image guided Interstitial Laser Ablation of breast tumors
Other Name: Novilase®

Primary Outcome Measures :
  1. Collect information on the proportion of tumors ablated for sample size calculations in the pivotal trial [ Time Frame: one month end point ]

    Evaluate the rate of complete tumor ablation by Novilase ILT of small breast cancers and characterize the correlation of imaging (MR, US, x-ray) in detecting residual post ablation with histopathology of the excised specimen.

    An individual patient will be considered to have a complete ablation if the pathology results post excision demonstrates that no visible gross residual tumor is present.

Secondary Outcome Measures :
  1. To gain experience with the cosmetic outcome and rate of recovery tools [ Time Frame: One month end point ]
    Evaluate satisfaction, utilizing the European Organization for Research and Treatment of Cancer Breast Cancer Specific Quality of Life Questionnaire (EORTC QLQ-BR23) survey and cosmetic outcome utilizing the physician-reported Four-Point Scoring System of Breast Cosmesis.

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Females 18 to 80 years of age
  • Tumor is well visualized through x-ray mammography or ultrasound imaging and amenable to image guidance therapy (a tumor which is well visualized through imaging can be identified from surrounding breast tissue and does not have margins
  • obscured by other structures or artifacts on the images)
  • Tumor must be well visualized (as defined above) on MRI
  • Definitive pathologic diagnosis by needle core biopsy
  • Unifocal malignant tumor that does not exceed 20mm in diameter and measures at least 5mm away from the skin and chest wall
  • Cluster of microcalcifications that do not exceed 10 mm in diameter and measures at least 5mm away from the skin and chest wall
  • Subjects with or without palpable lymph nodes
  • Subjects with mammographic appearance of overall dense parenchymal tissue may be included, as long as a clearly evident marker is present at tumor site
  • Subjects with less than 25% intraductal component
  • Subject has no clinically significant co-morbidities (i.e. chronic illnesses existing simultaneously with and usually independent of breast cancer) that affect life expectancy. Subject has given written informed consent
  • Subject agrees to comply with follow up visits

Exclusion Criteria:

  • Subjects younger than 18 years of age
  • Pregnant or breast-feeding women
  • Tumors poorly visualized by x-ray mammography or ultrasound imaging
  • Women who are morbidly obese (>300 lbs)
  • Acute or chronic severe renal insufficiency (Glomerular filtration rate (GFR) <30ml/min/1.73 sq.meters)
  • Moderate to end-stage kidney disease and a history of severe asthma or allergies
  • Tumors measuring greater than 20mm in diameter
  • Subjects with advanced stage breast cancer
  • Subjects with prior history of cancer in the ILT treated breast
  • Subjects with recurrent breast cancer
  • Subjects with lobular neoplasm, metastatic carcinoma to breast, sarcoma, Phylloides tumor, or Paget's disease
  • Subjects with benign vascular tumor
  • Subjects with benign lesions such as fibroadenoma, atypical ductal hyperplasia, sclerosing adenosis, Papilloma, fibrocystic disease of breast
  • Subjects with DCIS with microinvasion
  • Subjects with a cluster of microcalcifications whose diameter is larger than 10 mm.
  • Subjects with extensive intraductal component and other characteristics not well visualized by imaging studies
  • Subjects who are BRCA positive.
  • Inability to lie prone or supine for one hour
  • Currently participating or enrolled in another investigational treatment, device or drug study through follow up
  • Undergoing concurrent neoadjuvant therapies for breast cancer
  • Cardiac pacemaker or other metallic implants which would prevent patient from safely undergoing MRI scan

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01478438

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United States, Arizona
The Breast Center of Southern Arizona
Tucson, Arizona, United States, 85712
United States, Colorado
Rose Medical Center - Rose Breast Center
Denver, Colorado, United States, 80220
United States, Illinois
St. Alexius Breast Care of St. Alexius Medical Center
Bartlett, Illinois, United States, 60103
Advocate Lutheran General Hospital - Caldwell Breast Center
Park Ridge, Illinois, United States, 60068
United States, Maryland
Walter Reed National Military Medical Center
Bethesda, Maryland, United States, 20889
United States, New York
Columbia University Medical Center - Department of Surgery
New York, New York, United States, 10032
United States, Ohio
University of Toledo - Eleanor N. Dana Cancer Center Breast Care
Toledo, Ohio, United States, 43614
United States, Oklahoma
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States, 73126
United States, Wisconsin
Wheaton Franciscan Health System
Wauwatosa, Wisconsin, United States, 53226
United Kingdom
North Bristol NHS Trust: Southmead Hospital - The Breast Care Centre
Bristol, United Kingdom, BS10 5NB
Mid Essex Hospital Services NHS Trust: Broomfield Hospital - Breast Unit
Chelmsford, United Kingdom, CM1 7ET
Norfolk & Norwich University NHS Foundation Trusts: Norfolk and Norwich University Hospital
Norwich, United Kingdom, NR4 7UY
Sponsors and Collaborators
Novian Health Inc.
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Principal Investigator: Barbara Schwartzberg, MD Rose Medical Center - Rose Breast Center
Principal Investigator: Michael Shere, M.D. North Bristol NHS Trust: Southmead Hospital - The Breast Care Centre
Additional Information:
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Responsible Party: Novian Health Inc.
ClinicalTrials.gov Identifier: NCT01478438    
Other Study ID Numbers: BR-002
First Posted: November 23, 2011    Key Record Dates
Last Update Posted: March 3, 2021
Last Verified: March 2021
Keywords provided by Novian Health Inc.:
20mm in diameter
5mm away from the skin and chest
Additional relevant MeSH terms:
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