[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100630665":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":25,"locations":31,"responsibleParty":48,"collaborators":19,"id":50,"slug":51,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":52,"sex":58,"minAge":59,"maxAge":19,"enrollmentInfo":60,"targetDuration":19,"studyType":63,"phases":64,"briefSummary":66,"conditions":67,"keywords":19,"overallStatus":69,"whyStopped":19,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":79},{"fullName":5,"class":6},"University of Utah","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"At-home Paracentesis","EXPERIMENTAL","Participants receive an at-home-based paracentesis procedure, which may occur anytime following confirmation of eligibility.",[13],"Procedure: At-home Paracentesis",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"PROCEDURE","Paracentesis is a bedside procedure to obtain ascitic fluid from the peritoneum through needle aspiration, performed for both diagnostic and therapeutic purposes. The procedure involves needle insertion into the peritoneal cavity to remove fluid for analysis or to relieve symptoms from tense ascites.",[9],null,[21],{"name":22,"affiliation":23,"role":24},"Anna Beck, MD","Huntsman Cancer Institute","PRINCIPAL_INVESTIGATOR",[26],{"name":27,"role":28,"phone":29,"phoneExt":19,"email":30},"Susan Sharry","CONTACT","801-585-3453","susan.sharry@hci.utah.edu",[32],{"facility":33,"status":19,"city":34,"state":35,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Huntsman Cancer Institute at the University of Utah","Salt Lake City","Utah","84112","United States","US",{"type":40,"coordinates":41},"Point",[42,43],-111.89105,40.76078,{"lat":43,"lon":42},[46],{"name":27,"role":28,"phone":29,"phoneExt":19,"email":47},"Susan.sharry@hci.utah.edu",{"type":49,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100630665","at-home-paracentesis-for-women-with-cancer-related-malignant-ascites-paracentesis-100630665",false,"NCT07490626","At-Home Paracentesis for Women With Cancer-Related Malignant Ascites (Paracentesis)","A Pilot Study of At-Home Paracentesis for Women With Cancer-Related Malignant Ascites: A Decentralized Interventional Treatment Trial (Paracentesis)","Paracentesis","Inclusion Criteria:\n\n* Female aged ≥ 18 years\n* Has completed an initial clinic-based paracentesis procedure.\n* Confirmed diagnosis of cancer.\n* Symptoms related to ascites requiring procedure in the opinion of the investigator.\n* Eligible to receive an ultrasound-guided paracentesis procedure at home in the opinion of the investigator.\n* If applicable, participant is able to safely hold anticoagulant therapy per institutional standards prior to the procedure in the opinion of the investigator.\n* For participants of child-bearing potential, participant is following standard of care guidelines for contraception.\n* Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.\n\nExclusion Criteria:\n\n* Rapidly deteriorating condition or suspected bowel obstruction.\n* Large ventral hernias or prior complications from paracentesis.\n* Need for concurrent procedures requiring hospital resources.\n* Known lack of safe environment or inability to obtain sterile conditions at home.\n* Any condition that would, in the Investigator's judgment, contraindicate the participant's participation in the procedure or clinical study due to safety concerns or compliance with clinical study procedures. For example,\n* Medical, psychiatric, cognitive, or other conditions that may compromise the participant's ability to understand the participant information, give informed consent, comply with the study protocol or complete the study.","FEMALE","18 Years",{"count":61,"type":62},20,"ESTIMATED","INTERVENTIONAL",[65],"NA","The goal of this study is to evaluate the change in symptoms for women with cancer-related malignant ascites who complete an at-home paracentesis procedure.",[68],"Malignant Ascites","NOT_YET_RECRUITING","2026-03-23",{"date":72,"type":73},"2026-03-27","ACTUAL",{"date":75,"type":62},"2026-05",{"date":77,"type":62},"2028-07",{"name":5,"class":6},1]