[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100612347":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":34,"centralContacts":43,"locations":52,"responsibleParty":68,"collaborators":47,"id":71,"slug":72,"hasResults":73,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":47,"eligibilityCriteria":77,"healthyVolunteers":73,"sex":78,"minAge":79,"maxAge":80,"enrollmentInfo":81,"targetDuration":47,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":97,"whyStopped":47,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":102,"completionDateStruct":104,"leadSponsor":106,"locationsCount":107},{"fullName":5,"class":6},"General Hospital of Shenyang Military Region","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Terlipressin group","EXPERIMENTAL","Continuous intravenous infusion of terlipressin 2-4 mg every 12 hours.",[13],"Drug: 2-4 mg of terlipressin",{"label":15,"type":16,"description":17,"interventionNames":18},"Somatostatin group","ACTIVE_COMPARATOR","Continuous intravenous infusion of somatostatin 3 mg every 12 hours.",[19],"Drug: 3 mg of somatostatin",[21,28],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DRUG","2-4 mg of terlipressin","Participants receive 2-4 mg of terlipressin by continuous intravenous infusion every 12 hours, with a maximum treatment course of 5 days.",[9],[27],"Terlivaz",{"type":22,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"3 mg of somatostatin","Participants receive 3 mg of somatostatin by continuous intravenous infusion every 12 hours, with a maximum treatment course of 5 days.",[15],[33],"Stilamin",[35,39,41],{"name":36,"affiliation":37,"role":38},"Xingshun Qi, MD","Department of Gastroenterology, General Hospital of Northern Theater Command","PRINCIPAL_INVESTIGATOR",{"name":40,"affiliation":37,"role":38},"Qianqian Li",{"name":42,"affiliation":37,"role":38},"Rong Li",[44,49],{"name":36,"role":45,"phone":46,"phoneExt":47,"email":48},"CONTACT","18909881019",null,"xingshunqi@126.com",{"name":40,"role":45,"phone":50,"phoneExt":47,"email":51},"13940307473","1208594776@qq.com",[53],{"facility":54,"status":47,"city":55,"state":56,"zip":47,"country":57,"countryCode":58,"cosmosGeoPoint":59,"geoPoint":64,"contacts":65},"Department of Gastroenterology, General Hospital of Northern Theater Command (formerly called General Hospital of Shenyang Military Area)","Shenyang","Liaoning","China","CN",{"type":60,"coordinates":61},"Point",[62,63],123.43278,41.79222,{"lat":63,"lon":62},[66,67],{"name":36,"role":45,"phone":46,"phoneExt":47,"email":48},{"name":40,"role":45,"phone":50,"phoneExt":47,"email":51},{"type":38,"investigatorFullName":69,"investigatorTitle":70,"investigatorAffiliation":5,"oldNameTitle":47,"oldOrganization":47},"Xingshun Qi","Director of Department of Gastroenterology","100612347","terlipressin-vs-somatostatin-in-cirrhotic-patients-with-acute-gastrointestinal-bleeding-and-acute-kidney-injury-100612347",false,"NCT07252401","Terlipressin vs. Somatostatin in Cirrhotic Patients With Acute Upper Gastrointestinal Bleeding and Renal Dysfunction","Terlipressin vs. Somatostatin in Cirrhotic Patients With Acute Upper Gastrointestinal Bleeding and Renal Dysfunction: A Multicenter Randomized Controlled Trial","Inclusion Criteria:\n\n* patients have a definite diagnosis of live cirrhosis and AUGIB;\n* patients present with renal dysfunction at admission;\n* patients' age 18-70 years old;\n* patients or relatives can sign the informed consent form.\n\nExclusion Criteria:\n\n* patients have hepatorenal syndrome- acute renal injury (HRS-AKI);\n* patients have structural kidney injury;\n* patients have chronic kidney disease;\n* patients received kidney replacement therapy before enrollment;\n* patients have a history of liver transplantation or TIPS;\n* patients have acute liver failure or acute-on-chronic liver failure;\n* patients have hepatic or renal malignant tumor;\n* patients have severe diseases of the heart, lungs, and brain;\n* patients have contraindications for experimental drugs;\n* patients are in pregnancy or lactation;\n* patients participated in other clinical studies within 3 months before enrollment;\n* patients have other conditions that investigators deem unsuitable for enrollment in the study.","ALL","18 Years","70 Years",{"count":82,"type":83},64,"ESTIMATED","INTERVENTIONAL",[86],"NA","Acute upper gastrointestinal bleeding (AUGIB) is a common complication in the decompensated stage of liver cirrhosis, of which approximately 70% is acute variceal bleeding (AVB) caused by portal hypertension. Existing evidence suggests that both terlipressin and somatostatin can be used to control AUGIB in cirrhotic patients, but terlipressin may be the first-line treatment for cirrhotic patients with AUGIB complicated by renal dysfunction (RD). Herein, a multicenter randomized controlled trial (RCT) has been designed to compare the efficacy of terlipressin and somatostatin in the treatment of cirrhotic patients with AUGIB complicated by RD.",[89],"Liver Cirrhosis",[91,92,93,94,95,96],"terlipressin","somatostatin","liver cirrhosis","acute upper gastrointestinal bleeding","renal dysfunction","acute kidney injury","NOT_YET_RECRUITING","2026-08-14",{"date":100,"type":101},"2026-08-18","ACTUAL",{"date":103,"type":83},"2026-09-25",{"date":105,"type":83},"2028-03-31",{"name":5,"class":6},1]