[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"abdominal-compartment-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:abdominal-compartment-syndrome":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,39,73,103,128],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":38},"100538480","intraoperative-peak-airway-pressure-changes-on-postoperative-pulmonary-function-after-muscle-plication-100538480",false,"NCT06291389","Intraoperative Peak Airway Pressure Changes on Postoperative Pulmonary Function After Muscle Plication","Effects of Intraoperative Peak Airway Pressure Changes on Postoperative Pulmonary Function After Muscle Plication in Abdominoplasty Operations: A Randomized Double-Blind Trial","Inclusion Criteria:\n\n* age ranged between 20 and 50 years old,\n* American Society of Anesthesiologists (ASA) physical status classification I\n* came for abdominoplasty operation\n\nExclusion Criteria:\n\n* anemia or hemoglobin levels below 11g\u002Fdl\n* bleeding problems\n* cardiovascular disorders\n* restrictive and obstructive respiratory disease\n* abdominoplasty without plication.","ALL","20 Years","50 Years",{"count":20,"type":21},120,"ESTIMATED","OBSERVATIONAL","An abdominal panniculus excision procedure is known as an abdominoplasty (panniculectomy). Musculofascial plication is a crucial aspect of abdominoplasty, especially for patients with significant divarication of the recti muscles. This study aimed to evaluate the effect of intraoperative changes in peak airway pressure (PAP) after muscle plication on postoperative pulmonary function.",[25],"Abdominal Compartment Syndrome","RECRUITING","2026-01-04",{"date":29,"type":30},"2026-01-06","ACTUAL",{"date":32,"type":30},"2024-03-10",{"date":34,"type":21},"2026-12-15",{"name":36,"class":37},"Al-Azhar University","OTHER",1,{"id":40,"slug":41,"hasResults":11,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":50,"conditions":51,"keywords":58,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":38},"100567777","intra-abdominal-hypertension-and-abdominal-compartment-syndrome-in-patients-after-pancreatic-procedures-100567777","NCT06672601","Intra-abdominal Hypertension and Abdominal Compartment Syndrome in Patients After Pancreatic Procedures.","The HYPA Study: Intra-abdominal Hypertension and Abdominal Compartment Syndrome in Patients Undergoing Open and Robotic Pancreatic Procedures","HYPA","Inclusion Criteria:\n\n* Patients ≥ 18-year-old\n* Indication for elective pancreatic procedure\n* Written informed consent\n\nExclusion Criteria:\n\n* Patients \\\u003C18 years old.\n* Contraindication for urinary catheter placement.\n* Refusal to participate in the study.","18 Years",{"count":49,"type":21},150,"This study investigates the development of intra-abdominal hypertension and compartment syndrome in patients undergoing elective pancreatic procedures. Main objective is to determine the proportion of patients after pancreatic operation who develop elevated intra-abdominal pressure and assess its association with postoperative complication rates. Another goal of the study is to compare open versus robotic pancreatic procedures regarding the occurrence of intra-abdominal hypertension and abdominal compartment syndrome.",[52,25,53,54,55,56,57],"Intra Abdominal Pressure","Pancreatic Surgery","Pancreatic Fistula After Pancreaticoduodenectomy","Delayed Gastric Emptying","Anastomotic Leaks","Overload Fluid",[59,60,61,62],"Intra-abdominal hypertension","Compartment syndrome","Pancreatic surgery","Robotic surgery","NOT_YET_RECRUITING","2024-11-07",{"date":66,"type":30},"2024-11-08",{"date":68,"type":21},"2025-01-01",{"date":70,"type":21},"2028-03-31",{"name":72,"class":37},"Charles University, Czech Republic",{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":80,"sex":16,"minAge":4,"maxAge":81,"enrollmentInfo":82,"targetDuration":4,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":90,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":94,"lastUpdatePostDateStruct":95,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":38},"100513883","comparison-of-bladder-pressure-versus-regional-intestinal-tissue-oxygenation-in-infants-100513883","NCT05971264","Comparison of Bladder Pressure Versus Regional Intestinal Tissue Oxygenation in Infants","BPvsNIRS","Inclusion Criteria:\n\n* Prepped and consented for laparoscopic pyeloplasty or minimal PSARP with perineal or vestibular fistula or lateral thoracotomy for the correction of esophageal atresia\n* Age of 12 months old or less at operation\n* Legal custodian gives consent\n\nExclusion Criteria:\n\n* Anterior abdominal wall thickness greater than 12 mm measured on preoperative MRI imaging if available\n* Patients planned for additional intestinal surgeries or non-standard pyeloplasty, e.g. pyeloplasty with nephrostoma\n* Patients planned for laparoscopic pyeloplasty whose intraoperative urine sample shows pathological results\n* Patients with esophageal atresia who experience pulmonary decompensation and need urgent surgery for fistula clipping",true,"12 Months",{"count":83,"type":21},30,"INTERVENTIONAL",[86],"NA","The goal of this clinical trial is to learn more about intestinal regional oxygen saturation measurements made with near-infrared spectroscopy and bladder pressure measurements in infants without risk of intraabdominal hypertension. The main question it aims to answer is if - in comparison to bladder pressure - the regional intestinal oxygen saturation measured with near-infrared spectroscopy is stable in the muscle-relaxed, intubated patients and the awake and non-sedated patient.\n\nIn case of participation the bladder pressure and the regional intestinal oxygen saturation (measured with near-infrared spectroscopy) will each be measured once intraoperatively and once postoperatively. Patients included in this study will be undergoing an operation which necessitates muscle-relaxation, as well as an indwelling urinary catheter during the operation and for a short-time thereafter for other reasons than this study.",[89,25],"Intraabdominal Hypertension",[91,92,93],"Near infra-red spectroscopy","Bladder pressure","Intraabdominal pressure","2024-04-24",{"date":96,"type":30},"2024-04-25",{"date":98,"type":21},"2024-05-01",{"date":100,"type":21},"2026-06-30",{"name":102,"class":37},"University Children's Hospital, Zurich",{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":107,"acronym":108,"eligibilityCriteria":109,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":110,"targetDuration":4,"studyType":84,"phases":112,"briefSummary":113,"conditions":114,"keywords":117,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":38},"100365082","fasciotens-to-treat-an-open-abdomen---a-prospective-cohort-study-100365082","NCT04033614","Fasciotens to Treat an Open Abdomen - a Prospective Cohort Study","Fasciotens","Inclusion Criteria:\n\n* Laparostoma with a resorbable net and planned or necessary \"second look\" operation.\n* Age of majority\n* Signed informed consent form or in the case of patients unable to give consent, signature from the authorised representative\u002Flegal carevier or consultant.\n\nExclusion Criteria for the period of use of the Fasciotens Abdomen device:\n\n* Pregnancy or breast-feeding at the time of inclusion into the study\n* A Moribund patient with a life expectancy of less than 24 hours despite laparostomy\n* Unstable thorax or known severe skeletal instability which impaires the use of the fasciotens abdomen device.\n* Open wounds or infections at the potential contact points of the Fasciotens abdomen device\n* Known cardiac insufficiency with ejection fraction less than 35%\n* Patients with lung failure (ARDS) and the need for abdominal positioning within the next 24h\n\nExclusion criteria for the entire duration of the study:\n\n* Persons who are accommodated in a mental hospital or an insititution on official or judicial instruction\n* Persons who are dependent on or have an employment relationship with the principal investigator\n* Other conditions which, at the judgement of the investigator, militate against the use of the investigational product\n* Minority",{"count":111,"type":21},15,[86],"The open abdomen can occur as a result of various diseases. After infections of the abdomen, compartment syndromes or traumata, it is essential for survival (1). This condition of the open abdomen lasts from days to months. Within a very short time, the fascia and abdominal wall structures retract in such a way that direct abdominal closure is often impossible. In addition, there is a pronounced intraabdominal oedema, which additionally increases the space required by the abdominal organs. Therefore, it is clinically indispensable to increase the space of the intraabdominal organs in this life-threatening situation. After the laparotomy (opening of the abdomen) has been performed, it is therefore not closed. However, the natural traction on the abdominal wall, in particular on the fascia, the attached musculature as well as skin and subcutis, no longer exists in this situation. As a result, these structures retract over the period of the existing laparostoma.\n\nIn the present study, the CE-certified medical device Fasciotens Abdomen will be used to prove the functionality of this device and the user feasibility.\n\nThe basic principle of Fasciotens Abdomen is the ventrally directed pulling force on the two fascial edges via an external device with support on the thorax and pelvis. The possibility to apply a traction to the fascia from the moment of opening the abdomen without reducing the intraabdominal space is absolutely new and the rationale of this technique. The objective of this study is to prove the obvious prevention of fascial retraction through the Fasciotens Abdomen device.",[25,115,89,116],"Pancreatitis,Acute Necrotizing","Peritonitis",[118],"Laparotomy, open abdomen, fascia, retraction, intraabdominal oedema","2023-04-17",{"date":121,"type":30},"2023-04-19",{"date":123,"type":30},"2019-08-05",{"date":125,"type":21},"2026-08",{"name":127,"class":37},"RWTH Aachen University",{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":16,"minAge":47,"maxAge":4,"enrollmentInfo":135,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":137,"conditions":138,"keywords":141,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":152,"leadSponsor":154,"locationsCount":157},"100413896","physiologic-signals-and-signatures-with-the-accuryn-monitoring-system---the-accuryn-registry-100413896","NCT04669548","Physiologic Signals and Signatures With the Accuryn Monitoring System - The Accuryn Registry","Physiologic Signals and Signatures With the Accuryn Monitoring System - A Retrospective and Prospective Analysis (The Accuryn Registry)","Inclusion Criteria:\n\n1. Signed or Verbal Informed Consent as required by IRB (if applicable).\n2. Adult (age ≥ 18).\n3. Monitored on the Accuryn® Monitoring System during their procedure and ICU stay (for retrospective enrollment).\n4. Patient is undergoing cardiac surgical intervention(s).\n\nExclusion Criteria:\n\n1. Known history of advanced chronic kidney disease defined by an estimated glomerular filtration rate (eGFR) \\\u003C20 mL\u002Fmin\u002F1.73m2 within 30 days prior to procedure.\n2. The patient is unsuitable for the study, in the opinion of the investigator. This may include vulnerable patient populations such as pregnant women, prisoners ,or those detained in a penal institution.",{"count":136,"type":21},2500,"The Accuryn Registry Study is an open-ended, global, multi-center, retrospective and prospective, single-arm data collection study with an FDA cleared device. The target population are cardiovascular surgery patients. Physiologic data measurements will be collected from enrolled subjects using electronic medical records and data streams via the Accuryn Monitoring System.",[89,25,139,140],"Acute Kidney Injury","Cardiovascular Surgery",[142,143,140,144,145,146],"Acute Kidney Injury (AKI)","CABG","Intraabdominal Pressure (IAP)","Urine Output (UO)","Accuryn","2022-09-26",{"date":149,"type":30},"2022-09-28",{"date":151,"type":30},"2020-12-21",{"date":153,"type":21},"2026-12-31",{"name":155,"class":156},"Potrero Medical","INDUSTRY",9]