Ignite Creation Date:
2025-12-24 @ 5:06 PM
Ignite Modification Date:
2026-02-25 @ 6:58 PM
Study NCT ID:
NCT02009150
Status:
UNKNOWN
Last Update Posted:
2018-09-05
First Post:
2013-12-07
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Evaluation of a Novel Infra-red Breast Imaging System for Risk Assessment in Women at High Risk for Breast Cancer.
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D001943', 'term': 'Breast Neoplasms'}], 'ancestors': [{'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D001941', 'term': 'Breast Diseases'}, {'id': 'D012871', 'term': 'Skin Diseases'}, {'id': 'D017437', 'term': 'Skin and Connective Tissue Diseases'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'CASE_ONLY'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 236}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2014-04', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2018-09', 'completionDateStruct': {'date': '2018-10', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2018-09-03', 'studyFirstSubmitDate': '2013-12-07', 'studyFirstSubmitQcDate': '2013-12-07', 'lastUpdatePostDateStruct': {'date': '2018-09-05', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2013-12-11', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2017-07', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Diagnostic accuracy of 3D MIRA as a breast imaging aid in women with a high risk of breast cancer', 'timeFrame': 'up to 36 months'}], 'secondaryOutcomes': [{'measure': 'To test whether repetitive screening with 3D MIRA technology can provide information on the likelihood of developing breast cancer.', 'timeFrame': 'up to 36 months'}]}, 'conditionsModule': {'conditions': ['Breast Cancer']}, 'descriptionModule': {'briefSummary': "Three-dimensional functional Metabolic Imaging (3D MIRA) is a new infrared imaging technology using the Real Imager 4(RI4) developed by Real Imaging. This technology generates 3D metabolic maps and based on sophisticated machine learning technology, provides objective risk assessment for the presence of malignant tumor. The procedure is non-invasive, comfortable and does not involve ionizing radiation. Moreover, Real Imaging's 3D Functional MIRA is unaffected by breast density and is therefore ideal for evaluating patients with mammographically dense breasts.\n\nThe purpose of this clinical study is to assess the ability of this novel technology to detect clinically occult breast cancer in a cohort of women that are at high risk for breast cancer.\n\nWe hypothesize that the combination of screening mammography and metabolic screening (3D MIRA) will result in significantly higher breast cancer detection rates."}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '20 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'Women who are determined to have high risk of breast cancer and who are screened biannually by existing screening modalities (mammography, ultrasound or MRI)', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Female\n* Woman has read, understood and signed the inform consent form\n* Age: 20 years and older\n* Women who are asymptomatic for breast cancer\n* Proven carriers of deleterious BRCA1 or BRCA2 mutations Or Women that were found to have a lifetime risk of developing breast cancer greater or equal to 20% based on Tyrer-Cuzick, Gail or Clause risk models\n* Women scheduled to undergo routine mammography and/or US or MRI screening\n\nExclusion Criteria:\n\n* Women who have had a mammography and/or ultrasound examination performed on the day of the study prior to MIRA scan\n* Women who had a lumpectomy surgery\n* Women who had undergone mastectomy and/or reconstruction\n* Women who have undergone any type of breast surgery throughout the 6 months preceding the study\n* Women who have had a breast biopsy performed throughout the 10 weeks preceding the study.\n* Women who have a fever on the day of the MIRA imaging\n* Women who are pregnant\n* Women who are breast-feeding\n* Women who had undergone breast reduction/augmentation'}, 'identificationModule': {'nctId': 'NCT02009150', 'briefTitle': 'Evaluation of a Novel Infra-red Breast Imaging System for Risk Assessment in Women at High Risk for Breast Cancer.', 'organization': {'class': 'INDUSTRY', 'fullName': 'Real Imaging Ltd.'}, 'officialTitle': 'Evaluation of REAL IMAGING\'S 3D Functional Metabolic Imaging and Risk Assessment ("3D MIRA") System in Women at High Risk for Breast Cancer', 'orgStudyIdInfo': {'id': '960-CSP-ISR_HighRiskMC_ILS1'}}, 'armsInterventionsModule': {'armGroups': [{'label': 'Women at high risk for breast cancer', 'description': 'Proven carriers of deleterious BRCA1 or BRCA2 mutations Or Women that were found to have a lifetime risk of developing breast cancer greater or equal to 20% based on Tyrer-Cuzick, Gail or Clause risk models.'}]}, 'contactsLocationsModule': {'locations': [{'zip': '5262000', 'city': 'Ramat Gan', 'country': 'Israel', 'facility': 'The Chaim Sheba Medical Center at Tel-Hashomer', 'geoPoint': {'lat': 32.08227, 'lon': 34.81065}}], 'overallOfficials': [{'name': 'Miri Sklair-Levy, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'The Chaim Sheba Medical center at Tel-Hashomer'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Real Imaging Ltd.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}