Ignite Creation Date:
2025-12-24 @ 3:30 PM
Ignite Modification Date:
2025-12-26 @ 2:09 PM
Study NCT ID:
NCT01367392
Status:
COMPLETED
Last Update Posted:
2012-02-15
First Post:
2011-06-06
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Effectiveness and Safety of CT-guided Needle Placement in the Liver With the Aid of the ActiSight Needle Guidance System
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'interventionBrowseModule': {'meshes': [{'id': 'D001706', 'term': 'Biopsy'}], 'ancestors': [{'id': 'D003581', 'term': 'Cytodiagnosis'}, {'id': 'D003584', 'term': 'Cytological Techniques'}, {'id': 'D019411', 'term': 'Clinical Laboratory Techniques'}, {'id': 'D019937', 'term': 'Diagnostic Techniques and Procedures'}, {'id': 'D003933', 'term': 'Diagnosis'}, {'id': 'D013048', 'term': 'Specimen Handling'}, {'id': 'D003949', 'term': 'Diagnostic Techniques, Surgical'}, {'id': 'D013514', 'term': 'Surgical Procedures, Operative'}, {'id': 'D008919', 'term': 'Investigative Techniques'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE4'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 20}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2011-06'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2012-02', 'completionDateStruct': {'date': '2012-01', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2012-02-14', 'studyFirstSubmitDate': '2011-06-06', 'studyFirstSubmitQcDate': '2011-06-06', 'lastUpdatePostDateStruct': {'date': '2012-02-15', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2011-06-07', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2012-01', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'accuracy', 'timeFrame': 'during the procedure', 'description': 'Frequency of placing the needle at a location suitable for the planned intervention, as determined by the investigator reviewing the CT images.'}], 'secondaryOutcomes': [{'measure': 'time', 'timeFrame': 'during the procedure', 'description': 'Total CT-Guided procedure time, starting with scan for entry point planning;'}, {'measure': 'time', 'timeFrame': 'during the procedure', 'description': 'Time required to guide the needle to the target'}, {'measure': 'radiation', 'timeFrame': 'during the procedure', 'description': 'Subject radiation exposure during the procedure'}, {'measure': 'total number of scans', 'timeFrame': 'during the procedure', 'description': 'Number of CT scans during the procedure'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'conditions': ['Accurate Navigation to the Lesion']}, 'descriptionModule': {'briefSummary': 'The purpose of this study is to confirm the safety and effectiveness of the ActiSight™ Needle Guidance System with CT-guided percutaneous (through the skin) liver biopsies and ablations . The device used in this study is designed to assist the physician in guiding the needle towards the suspected area. This device does not change the procedure of liver biopsy or ablation. The only difference is that a small adhesive pad is placed on the skin and a miniature video camera is attached to the end of the needle. This camera does not enter the body.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '80 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Male or non-pregnant female subjects, between the ages of 18 and 80 at the time of enrollment.\n* Subjects scheduled for clinically indicated CT guided percutaneous needle placements in the liver who meet the desired target population described above.\n* Written informed consent to participate in the study.\n* Ability to comply with the requirements of the study procedures.\n* Verified home address and phone number to facilitate study follow-up.\n\nExclusion Criteria:\n\n* Significant coagulopathy that cannot be adequately corrected.\n* Subjects who participated in an active stage of any drug, intervention or treatment trial within 30 days of enrollment.\n* Subjects with preexisting conditions, which, in the opinion of the investigator, interfere with the conduct of the study.\n* Subjects who are uncooperative or cannot follow instructions.\n* Mental state that may preclude completion of the study procedure.\n* Pregnant or nursing female subjects.'}, 'identificationModule': {'nctId': 'NCT01367392', 'briefTitle': 'Effectiveness and Safety of CT-guided Needle Placement in the Liver With the Aid of the ActiSight Needle Guidance System', 'organization': {'class': 'INDUSTRY', 'fullName': 'ActiViews Ltd.'}, 'officialTitle': 'Confirmation of Clinical Effectiveness and Safety of CT-guided Needle Placement in the Liver With the Aid of the ActiSight Needle Guidance System', 'orgStudyIdInfo': {'id': 'ACST-2011-1'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'interventional procedure', 'description': 'The patients undergo the required interventional procedure, biopsy or ablation', 'interventionNames': ['Device: biopsy or ablation']}], 'interventions': [{'name': 'biopsy or ablation', 'type': 'DEVICE', 'description': 'biopsy or ablation performed as in standard of care with assistance of ActiSight Needle Guidance system', 'armGroupLabels': ['interventional procedure']}]}, 'contactsLocationsModule': {'locations': [{'city': 'Montreal', 'state': 'Quebec', 'country': 'Canada', 'facility': 'Royal Victoria Hospital', 'geoPoint': {'lat': 45.50884, 'lon': -73.58781}}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'ActiViews Ltd.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}