[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100449960":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":27,"centralContacts":31,"locations":36,"responsibleParty":54,"collaborators":57,"id":61,"slug":62,"hasResults":63,"nctId":64,"briefTitle":65,"officialTitle":66,"acronym":24,"eligibilityCriteria":67,"healthyVolunteers":63,"sex":68,"minAge":69,"maxAge":24,"enrollmentInfo":70,"targetDuration":24,"studyType":73,"phases":74,"briefSummary":76,"conditions":77,"keywords":24,"overallStatus":38,"whyStopped":24,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"Dartmouth-Hitchcock Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"CONVIVO system","EXPERIMENTAL","During tumor resection, study investigators trained in the use of the system will determine when the CONVIVO imaging system will be used for in vivo¬ imaging. At this point 5 mg\u002Fkg of fluorescein will be administered intravenously by an anesthesia provider over one minute.Approximately 2-5 minutes following administration of FNa in situ imaging will be performed by the participating surgeon ensuring proper technique.",[13],"Diagnostic Test: CONVIVO system",{"label":15,"type":6,"description":16,"interventionNames":17},"Conventional histologic evaluation","Following image acquisition, the tissue region imaged with the CONVIVO system will then be biopsied using biopsy forceps. This will be passed immediately off the surgical field as a research specimen and provided to a member of the research team to be prepared for conventional histologic evaluation. The specimen will be labeled with the deidentified subject and sample number. This sequence will then be repeated for each successive sample.",[18],"Other: Conventional histologic evaluation",[20,25],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":24},"DIAGNOSTIC_TEST","Approximately 2-5 minutes following administration of FNa in situ imaging will be performed by the participating surgeon ensuring proper technique. Prior to entering the surgical field, the probe will be covered in a disposable sterile sheath that is manufactured with quality assurance for this purpose. The probe will gently be held against the tissue interface while imaging occurs. Again this will only be in regions that would normally be resected or sampled in routine clinical care. Following image acquisition, a neuropathologist present in the operating room, will review and capture each image.",[9],null,{"type":6,"name":15,"description":16,"armGroupLabels":26,"otherNames":24},[15],[28],{"name":29,"affiliation":5,"role":30},"Linton T Evans, MD","PRINCIPAL_INVESTIGATOR",[32],{"name":29,"role":33,"phone":34,"phoneExt":24,"email":35},"CONTACT","603-650-5026","Linton.T.Evans@hitchcock.org",[37],{"facility":5,"status":38,"city":39,"state":40,"zip":41,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"RECRUITING","Lebanon","New Hampshire","03756","United States","US",{"type":45,"coordinates":46},"Point",[47,48],-72.25176,43.64229,{"lat":48,"lon":47},[51,53],{"name":29,"role":33,"phone":34,"phoneExt":24,"email":52},"linton.t.evans@hitchcock.org",{"name":29,"role":30,"phone":24,"phoneExt":24,"email":24},{"type":30,"investigatorFullName":55,"investigatorTitle":56,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"Linton T. Evans","Principle Investigator",[58],{"name":59,"class":60},"Carl Zeiss Meditec, Inc.","INDUSTRY","100449960","evaluation-of-the-convivo-system-100449960",false,"NCT05139277","Evaluation of the CONVIVO System","Clinical Investigation to Evaluate the CONVIVO System for Discrimination of Normal From Abnormal Tissue During Brain Tumor Resection","Inclusion Criteria:\n\n* Adult patients (age\\>18)\n* Adults presenting with suspected intracranial gliomas (including glioblastoma), cerebral metastasis, meningiomas, acoustic neuromas, and pituitary adenomas, who are surgical candidates\n* Adults able to provide informed consent.\n\nExclusion Criteria:\n\n* Pregnancy\n* Children (age \\\u003C18 years)\n* Fluorescein sodium (FNa) allergy","ALL","18 Years",{"count":71,"type":72},30,"ESTIMATED","INTERVENTIONAL",[75],"NA","The primary objective of this study is to evaluate the diagnostic performance of the CONVIVO confocal endomicroscope in discriminating between normal and abnormal tissue in vivo during brain tumor surgery. The interpretation of intraoperative images obtained in situ will be tested against conventional histologic evaluation of targeted biopsies from imaged tissue. The study team hypothesize that there will be a high degree of correlation between images obtained with the CONVIVO system and conventional histologic interpretation.",[78,79,80,81,82,83],"Glioblastoma","Glial Tumor","Brain Metastases","Meningioma","Schwannoma","Pituitary Tumor","2026-02-04",{"date":86,"type":87},"2026-02-06","ACTUAL",{"date":89,"type":87},"2022-06-28",{"date":91,"type":72},"2026-10",{"name":5,"class":6},1]