[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ascites-malignant\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ascites-malignant":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":26,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100495097","qol-and-sarcopenia-in-patients-with-ascites-100495097",false,"NCT05726747","QOL and Sarcopenia in Patients With Ascites","Health-related Quality of Life Outcomes and Changes in Sarcopenia in Patients With Refractory Ascites","Inclusion Criteria:\n\n1. Age \\>\u002F=18\n2. Eastern Cooperative Oncology Group (ECOG) performance score \\\u003C 3\n3. Refractory ascites due to cirrhosis or malignancy, requiring more than 1 therapeutic paracentesis in a 6 week period within 3 months of enrollment.\n4. Capable of giving informed consent\n\nExclusion Criteria:\n\n1. Life expectancy less than 3 months\n2. Unable to participate in neuropsychological tests\u002Fquestionnaires\n3. Pregnant or nursing women. .","ALL","18 Years",{"count":19,"type":20},70,"ESTIMATED","OBSERVATIONAL","Clinical data regarding quality of life in patients with refractory ascites is limited and preceded the development of newer questionnaires that may be more robust. One primary objective of this study is to study changes in quality in life in a prospective fashion using newer general and ascites-specific quality of life survey instruments specific to benign and malignant etiologies.\n\nSarcopenia is a condition that is prevalent in cancer and cirrhosis. Current data is retrospective and associative, evaluating heterogeneous patient populations at different stages within the timeline of refractory ascites. The other primary objective of this study is to study sarcopenia in a prospective fashion and to understand its kinetics once a patient develops refractory ascites.\n\nProspectively-obtained measures of deterioration in patient-reported outcomes and in muscle mass will form the basis for the next stage of investigation of interventions to mitigate these declines.",[24,25],"Ascites Hepatic","Ascites, Malignant",[27,28],"ascites","sarcopenia","RECRUITING","2026-06-12",{"date":32,"type":33},"2026-06-15","ACTUAL",{"date":35,"type":33},"2023-05-23",{"date":37,"type":20},"2027-10",{"name":39,"class":40},"Abramson Cancer Center at Penn Medicine","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":53,"phases":54,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":41},"100574421","phase-1-intraperitoneal-immune-checkpoint-inhibitors-and-zoledronic-acids-for-gastric-cancer-malignant-ascites-100574421","NCT06759064","Intraperitoneal Immune Checkpoint Inhibitors and Zoledronic Acids for Gastric Cancer Malignant Ascites","Efficacy and Safety of Intraperitoneal Immune Checkpoint Inhibitors and Zoledronic Acids in Gastric Cancer Malignant Ascites: a Phase I\u002FII Clinical Study (IPIZA)","IPIZA","Inclusion Criteria:\n\n* Gastric adenocarcinoma diagnosed pathologically;\n* Malignant ascites confirmed by ascites cytology;\n* Presence of ascites confirmed by CT with ascites graded as 2nd and 3rd degree (EASL guidelines and ICA consensus);\n* Those aged 18-75 years;\n* Patients who had not undergone local administration of drugs in the abdominal cavity and systemic immunotherapy within the previous 4 weeks;\n* Vital signs are stable, Karnofsky score (≥70), and expected survival time is \\>3 months;\n* Normal bone marrow haematopoietic function, blood routine: HGB ≥90g\u002FL, WBC ≥2.5×10\\^9\u002FL (NEU ≥1.5×10\\^9\u002FL), PLT ≥90×10\\^9\u002FL;\n* Normal coagulation function without bleeding tendency (International normalised ratio of prothrombinogen INR\\\u003C1.5);\n* Liver function: total bilirubin ≤1.5 times the upper limit of normal (ULN); AST and ALT ≤2 times the upper limit of normal (ULN) (or ≤5 times the upper limit of normal (ULN) if the abnormalities are mainly due to tumour infiltration);\n* Renal function: Cr ≤1.5 times the upper limit of normal (ULN) or creatinine clearance ≥60mL\u002Fmin.\n\nExclusion Criteria:\n\n* Non-malignant ascites (e.g., portal hypertension ascites or infected ascites);\n* Presence of contraindications to immunotherapy (including long-term hormone use, history of radiation pneumonitis, radiation hepatitis, radiation enteritis, etc.);\n* Combination of other serious cardiopulmonary diseases that affect the treatment, etc;\n* Patients with extensive abdominal adhesions; encapsulated peritoneal fluid; history of intestinal obstruction; and malignant patients with extensive distant metastases in the terminal stage;\n* Women who are breastfeeding, pregnant, or preparing for pregnancy;\n* Patients with plasma albumin (ALB) \\\u003C30 g\u002FL and severe hypoproteinemia;\n* Patients with known hypersensitivity to components of the test drug or its analogues;\n* Patients with other severe, acute or chronic diseases that may interfere with the interpretation of the study results and who, in the judgement of the investigator, are unsuitable for participation in the clinical trial;\n* Patients with cognitive dysfunction, or poor treatment compliance as judged by the investigator;\n* Participants in other clinical trials within 4 weeks;\n* Combination of other malignancies;\n* Those who, in the opinion of the investigator, are not suitable for participation in the clinical trial.","75 Years",{"count":52,"type":20},24,"INTERVENTIONAL",[55,56],"PHASE1","PHASE2","This study is to evaluate the safety and efficacy of intraperitoneal injection of immune checkpoint inhibitor combined with zoledronic acid for the treatment of malignant ascites in gastric cancer.\n\nThis study is a phase Ib\u002FII clinical study to evaluate the safety and efficacy of intraperitoneal injection of immune checkpoint inhibitors in combination with zoledronic acid in the treatment of malignant ascites in gastric cancer, which consists of two phases, firstly, the phase Ib safety study, which adopts the '3+3' drug-escalation experimental design, and after determining the safe and tolerable dose, it will proceed to the second part of the phase II efficacy study. The Phase II study was designed by Simon's two-stage approach to evaluate the efficacy of immune checkpoint inhibitors in combination with zoledronic acid in the treatment of malignant ascites in gastric cancer.",[59,25],"Cancer of Stomach, Adenocarcinoma",[61,62,63,64,65],"gastric cancer","malignant ascites","Immune checkpoint inhibitors","zoledronic acid","intraperitoneal injection","2025-11-15",{"date":68,"type":33},"2025-11-19",{"date":70,"type":33},"2024-09-12",{"date":72,"type":20},"2026-09-01",{"name":74,"class":40},"Qilu Hospital of Shandong University"]