[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100530095":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":31,"centralContacts":41,"locations":50,"responsibleParty":68,"collaborators":31,"id":72,"slug":73,"hasResults":74,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":31,"eligibilityCriteria":78,"healthyVolunteers":74,"sex":79,"minAge":80,"maxAge":31,"enrollmentInfo":81,"targetDuration":31,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":53,"whyStopped":31,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"University of California, Los Angeles","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"SBO treated without NG tube","EXPERIMENTAL","Patients who decline NG intubation will be enrolled in the trial, followed prospectively and have the same outcome measures as are acquired in the other study arms.",[13],"Procedure: SBO Treatment Without NG Tubes",{"label":15,"type":10,"description":16,"interventionNames":17},"SBO treated with NG tube and Water-Soluble Contrast (WSC)","Patients who select NG tube treatment will be randomized into experimental and control groups. The experimental groups will have 100 cc of WSC administered in the NG tube within 2 hours of NG tube placement.",[18],"Drug: Gastrografin",{"label":20,"type":21,"description":22,"interventionNames":23},"SBO Treated with NG tube and Placebo","PLACEBO_COMPARATOR","The control group will have 100cc of saline administered via the NG tube within 2 hours of NG tube placement.",[24],"Drug: Saline",[26,32,36],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"DRUG","Gastrografin","Administration of WSC (Gastrografin) 2 hours after placement of NGT.",[15],null,{"type":27,"name":33,"description":34,"armGroupLabels":35,"otherNames":31},"Saline","Administration of Saline 2 hours after placement of NGT.",[20],{"type":37,"name":38,"description":39,"armGroupLabels":40,"otherNames":31},"PROCEDURE","SBO Treatment Without NG Tubes","Patients who decline to have NG tubes placed will be enrolled and followed with the same outcomes protocol as the other patients in the trial",[9],[42,47],{"name":43,"role":44,"phone":45,"phoneExt":31,"email":46},"Steven Stokes","CONTACT","310-206-7436","sstokes@mednet.ucla.edu",{"name":48,"role":44,"phone":49,"phoneExt":31,"email":31},"Edward H Livingston, MD","310-794-7788",[51],{"facility":52,"status":53,"city":54,"state":55,"zip":56,"country":57,"countryCode":58,"cosmosGeoPoint":59,"geoPoint":64,"contacts":65},"University of California, Los Angeles, David Geffen School of Medicine","RECRUITING","Los Angeles","California","90024","United States","US",{"type":60,"coordinates":61},"Point",[62,63],-118.24368,34.05223,{"lat":63,"lon":62},[66],{"name":31,"role":44,"phone":67,"phoneExt":31,"email":31},"310-825-2631",{"type":69,"investigatorFullName":70,"investigatorTitle":71,"investigatorAffiliation":5,"oldNameTitle":31,"oldOrganization":31},"PRINCIPAL_INVESTIGATOR","Edward Harry Livingston","Professor of Surgery","100530095","phase-3-optimizing-treatment-of-adhesive-small-bowel-obstruction-100530095",false,"NCT06182319","Optimizing Treatment of Adhesive Small Bowel Obstruction","The Use of Nasogastric Tubes And Water-Soluble Contrast In The Management Of Small Bowel Obstruction: A Feasibility Study","Inclusion Criteria:\n\n1. Male or female ≥18 years of age.\n2. Documentation of aSBO as evidenced by one or more clinical features meeting the following criteria: Nausea, emesis, abdominal pain, distended abdomen CT evidence of aSBO\n\nExclusion Criteria:\n\n1. Pregnant, breastfeeding, or unwilling to practice birth control during participation in the study.\n2. Presence of a condition or abnormality that in the opinion of the investigator would compromise the safety of the patient or the quality of the data.\n3. Unstable angina or recent myocardial infarction (MI)\u002Fstroke within 6 months\n4. Nonadhesive SBO\n\n   1. Paralytic Ileus\n   2. Incarcerated hernia\n   3. Fecal impaction\n   4. Intra-abdominal malignancy Early aSBO within 4 weeks of a prior abdominal operation","ALL","18 Years",{"count":82,"type":83},40,"ESTIMATED","INTERVENTIONAL",[86],"PHASE3","Small bowel obstruction (SBO) is one of the most common causes of serious gastrointestinal disease in the US. Adhesion-related SBO (aSBO) is usually treated by the placement of a nasogastric tube (NGT) to decompress the stomach, administration of intravenous (IV) fluids and observation by a surgical team.\n\nThe purpose of this feasibility study is to determine the potential for implementation of treatment protocols for aSBO and determine the feasibility of randomizing patients with aSBO to receive or not receive NGTs or water-soluble contrast (WSC). The investigators will also determine the ability to measure HRQOL as a main outcome for the treatment of aSBO. The studies outlined in this research program intend to address gaps in knowledge about how to determine who benefits from NGT placement, who can be managed without them, how to objectively determine when a bowel obstruction has resolved, how to reintroduce feeding to patients with aSBO, what criteria should be used for hospital discharge and what role cathartics such as WSC contrast have in the management of aSBO.\n\nThis feasibility study will enroll a limited number of patients (n=40) who will be followed for up to 30 days.",[89],"Adhesive Small Bowel Obstruction",[91,92,93,94],"nasogastric tube (NGT)","water-soluble contrast (WSC)","Adhesion-related SBO (aSBO)","Small bowel obstruction (SBO)","2024-05-07",{"date":97,"type":98},"2024-05-08","ACTUAL",{"date":100,"type":98},"2024-01-01",{"date":102,"type":83},"2025-12-15",{"name":5,"class":6},1]