[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100480360":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":26,"centralContacts":30,"locations":40,"responsibleParty":57,"collaborators":25,"id":59,"slug":60,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":64,"acronym":25,"eligibilityCriteria":65,"healthyVolunteers":61,"sex":66,"minAge":67,"maxAge":25,"enrollmentInfo":68,"targetDuration":25,"studyType":71,"phases":72,"briefSummary":74,"conditions":75,"keywords":25,"overallStatus":43,"whyStopped":25,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"Montefiore Medical Center","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Standard technique","ACTIVE_COMPARATOR","The conventional hollow bore needle on a syringe will be used",[13],"Procedure: Central venous catheter insertion",{"label":15,"type":16,"description":17,"interventionNames":18},"Peripheral IV","EXPERIMENTAL","A peripheral intravenous catheter will be used to obtain initial central venous access",[13],[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"PROCEDURE","Central venous catheter insertion","The clinical team will use the technique to establish central venous access",[15,9],null,[27],{"name":28,"affiliation":5,"role":29},"Benjamin J Friedman, MD","PRINCIPAL_INVESTIGATOR",[31,36],{"name":32,"role":33,"phone":34,"phoneExt":25,"email":35},"Joe Offenbacher, MD","CONTACT","646-929-7815","joseph.offenbacher@nyulangone.org",{"name":37,"role":33,"phone":38,"phoneExt":25,"email":39},"Benjamin Friedman, MD","718-920-6626","bfriedm@montefiore.org",[41],{"facility":42,"status":43,"city":44,"state":45,"zip":46,"country":47,"countryCode":48,"cosmosGeoPoint":49,"geoPoint":54,"contacts":55},"Montefiore","RECRUITING","The Bronx","New York","10467","United States","US",{"type":50,"coordinates":51},"Point",[52,53],-73.86641,40.84985,{"lat":53,"lon":52},[56],{"name":37,"role":33,"phone":25,"phoneExt":25,"email":25},{"type":58,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR","100480360","phase-4-central-line-study-100480360",false,"NCT05534971","Central Line Study","A Randomized Study Comparing Two Techniques for Central Venous Catheter Insertion","Inclusion Criteria:\n\nAdult patients in the emergency department who require ultrasound guided central line placement are eligible for participation and will be referred for participation in the study by the clinical team.\n\nExclusion Criteria:\n\n* Inherited, acquired, or medication related coagulopathy or thrombocytopenia (platelets \\\u003C 100,000). Patients will not be excluded for use of aspirin or other anti-platelet medication.\n* Previous central venous access at the same anatomical site.\n* Any indwelling catheter or wire that could potentially interfere with central line placement\n* Anterior border of the target vein deeper than 3.5cm\n\nOr for any clinical feature that would interfere with obtaining informed consent including dementia, delirium, or encephalopathy, as determined by the clinical attending physician.","ALL","18 Years",{"count":69,"type":70},160,"ESTIMATED","INTERVENTIONAL",[73],"PHASE4","Two different techniques for placing a central venous catheter will be compared. The studyu team hypothesizes that clinicians randomized to the peripheral catheter technique will have higher first attempt success rates, fewer procedural complications, and a shorter mean time to procedure completion than physicians assigned to wire through hollow bore needle.",[76],"Shock","2026-01-03",{"date":79,"type":80},"2026-01-06","ACTUAL",{"date":82,"type":80},"2022-11-16",{"date":84,"type":70},"2027-12",{"name":5,"class":6},1]