[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100533370":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":25,"locations":31,"responsibleParty":53,"collaborators":20,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":20,"eligibilityCriteria":62,"healthyVolunteers":63,"sex":64,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":20,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":20,"overallStatus":34,"whyStopped":20,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},{"fullName":5,"class":6},"Children's National Research Institute","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients Undergoing Augmented Reality Image-Guided Needle Procedures","EXPERIMENTAL","Patients will undergo their standard of care image-guided needle biopsy, aspiration, or injection with the Augmented Reality system. Patients will be monitored for adverse events for two weeks following their procedure.",[13],"Device: Augmented Reality System",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","Augmented Reality System","Subjects will undergo image guided needle aspiration, injection, or biopsy facilitated by the Augmented Reality system. The Augmented Reality guidance system will be operated by the interventional radiologist in the MRI suite.",[9],null,[22],{"name":23,"affiliation":5,"role":24},"Karun Sharma, MD, PhD","PRINCIPAL_INVESTIGATOR",[26],{"name":27,"role":28,"phone":29,"phoneExt":20,"email":30},"Emily Leibold, BSE","CONTACT","202-476-5522","eleibold@childrensnational.org",[32],{"facility":33,"status":34,"city":35,"state":36,"zip":37,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":46},"Children's National Hospital","RECRUITING","Washington D.C.","District of Columbia","20010","United States","US",{"type":41,"coordinates":42},"Point",[43,44],-77.03637,38.89511,{"lat":44,"lon":43},[47,50,51],{"name":23,"role":28,"phone":48,"phoneExt":20,"email":49},"202-476-3791","kvsharma@childrensnational.org",{"name":27,"role":28,"phone":29,"phoneExt":20,"email":30},{"name":52,"role":24,"phone":20,"phoneExt":20,"email":20},"Karun Sharma, MD\u002FPhD",{"type":24,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"Karun Sharma MD","Director of Interventional Radiology","100533370","augmented-reality-for-mri-guided-interventions-100533370",false,"NCT06224933","Augmented Reality For MRI-Guided Interventions","Augmented Reality Real-Time Guidance for MRI-Guided Interventions","Inclusion Criteria:\n\n* Provision of signed and dated informed consent form\n* Stated willingness to comply with all study procedures and availability for the duration of the study\n* Male or female, ages 3 to 21\n* Patient referred to Interventional Radiology for image-guided needle injection, aspiration, or biopsy.\n\nExclusion Criteria:\n\n* Patients who are unable to give informed consent themselves or through their parents.\n* Patients under 3 years of age\n* Patients over 300 pounds.\n* Patients who are claustrophobic and unable to tolerate MRI-guided procedure.\n* Contraindications to MRI such as MR-unsafe implants.",true,"ALL","3 Years","21 Years",{"count":68,"type":69},25,"ESTIMATED","INTERVENTIONAL",[72],"NA","The purpose of this study is to determine feasibility and safety of using an augmented reality system in patients undergoing MRI-Guided needle procedures.",[75,76,77],"Infections","Pain","Diagnosis","2025-08-28",{"date":80,"type":81},"2025-09-05","ACTUAL",{"date":83,"type":81},"2024-02-06",{"date":85,"type":69},"2026-05-31",{"name":5,"class":6},1]