[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100570077":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":32,"centralContacts":36,"locations":46,"responsibleParty":102,"collaborators":104,"id":136,"slug":40,"hasResults":137,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":141,"eligibilityCriteria":142,"healthyVolunteers":137,"sex":143,"minAge":144,"maxAge":40,"enrollmentInfo":145,"targetDuration":40,"studyType":148,"phases":149,"briefSummary":151,"conditions":152,"keywords":157,"overallStatus":67,"whyStopped":40,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":172},{"fullName":5,"class":6},"Xijing Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention: iNO Group","EXPERIMENTAL","Patients will receive 80 parts per million (ppm) NO during CPB through the oxygenator. After weaning of CPB, test gases will be delivered via inspiration limb of ventilator at a dose range of 40-80 ppm until 6 hours after ICU admission or until extubation after surgery, whichever comes first.",[13],"Drug: Nitric Oxide Gas",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard Care\u002FControl Group","PLACEBO_COMPARATOR","Patients in this group will receive standard care and 80 ppm nitrogen (N2, control group) are added to the gas mixture as control. In the circumstances when the N2 is not applicable, such as when the plasma-chemical NO synthesis device is employed for NO generatiaon and delivery, the device will be connected to the CPB and ventilator circuits, but the synthesis will remain inactive in the control group. Consequently, the circuit will be supplied with air devoid of NO.",[19],"Drug: Standard Care Arm",[21,27],{"type":22,"name":23,"description":11,"armGroupLabels":24,"otherNames":25},"DRUG","Nitric Oxide Gas",[9],[26],"Nitric Oxide inhalation",{"type":22,"name":28,"description":17,"armGroupLabels":29,"otherNames":30},"Standard Care Arm",[15],[31],"Nitrogen inhalation",[33],{"name":34,"affiliation":5,"role":35},"Chong Lei, M.D., & phd","PRINCIPAL_INVESTIGATOR",[37,42],{"name":34,"role":38,"phone":39,"phoneExt":40,"email":41},"CONTACT","18629011362",null,"crystalleichong@126.com",{"name":43,"role":38,"phone":44,"phoneExt":40,"email":45},"ziyu Zheng, ph.D.","13228082320","zhengziyu@126.com",[47,66,86],{"facility":48,"status":49,"city":50,"state":51,"zip":52,"country":53,"countryCode":54,"cosmosGeoPoint":55,"geoPoint":60,"contacts":61},"Massachusetts General Hospital, Department of Anesthesia, Critical Care and Pain Medicine","NOT_YET_RECRUITING","Boston","Massachusetts","02114","United States","US",{"type":56,"coordinates":57},"Point",[58,59],-71.05977,42.35843,{"lat":59,"lon":58},[62],{"name":63,"role":38,"phone":64,"phoneExt":40,"email":65},"Lorenzo Berra, M.D.","6176437733","lberra@mgh.harvard.edu",{"facility":5,"status":67,"city":68,"state":69,"zip":70,"country":71,"countryCode":72,"cosmosGeoPoint":73,"geoPoint":77,"contacts":78},"RECRUITING","Xi'an","Shaanxi","710032","China","CN",{"type":56,"coordinates":74},[75,76],108.92861,34.25833,{"lat":76,"lon":75},[79,82],{"name":80,"role":38,"phone":81,"phoneExt":40,"email":41},"Chong Lei, MD & phD","86-18629011362",{"name":83,"role":38,"phone":84,"phoneExt":40,"email":85},"Zefei Zhang, M.D.","86-18811797795","zzfanita7@163.com",{"facility":87,"status":49,"city":88,"state":40,"zip":89,"country":90,"countryCode":91,"cosmosGeoPoint":92,"geoPoint":96,"contacts":97},"Cardiology Research Institute, Tomsk National Research Medical Center","Tomsk","634012","Russia","RU",{"type":56,"coordinates":93},[94,95],84.98216,56.50049,{"lat":95,"lon":94},[98],{"name":99,"role":38,"phone":100,"phoneExt":40,"email":101},"Nikolay O. Kamenshchikov, M.D.","79138183657","nikolajkamenof@mail.ru",{"type":35,"investigatorFullName":80,"investigatorTitle":103,"investigatorAffiliation":5,"oldNameTitle":40,"oldOrganization":40},"Principal Investigator",[105,108,110,112,114,116,118,120,122,124,126,128,130,132,134],{"name":106,"class":107},"Nikolay O. Kamenshchikov., M.D., Tomsk National Research Medical Center of the Russian Academy of Sciences","UNKNOWN",{"name":109,"class":107},"Lorenzo Berra., M.D., Massachusetts General Hospital",{"name":111,"class":107},"Jiange Han, Tianjin Chest Hospital, Tianjin, China",{"name":113,"class":107},"Qingping Wu, Wuhan Union Hospital, Wuhan, China",{"name":115,"class":107},"Evgeniy Grigoriev, Research Institute for Complex Issues of Cardiovascular Diseases, Kemerovo, Russian Federation",{"name":117,"class":107},"Vladimir Boboshko, E. Meshalkin National Medical Research Center, Novosibirsk, Russian Federation",{"name":119,"class":107},"Andrei Bautin, The Almazov National Medical Research Centre, St. Petersburg, Russian Federation",{"name":121,"class":107},"Vladimir Pichugin, Specialized Cardiac Surgery Clinical Hospital named after Academician B.A. Korolev, Nizhny Novgorod, Russian Federation",{"name":123,"class":107},"Evgeniy Rosseykin, Federal Center of Cardiovascular Surgery, Khabarovsk, Russian Federation",{"name":125,"class":107},"Jing Shi, The Afffliated Hospital of Guizhou Medical University, Guiyang, China.",{"name":127,"class":107},"Grigoryev Evgeny, Scientific Research Insitute for Complex Issues of Cardiovascular Diseases, Kemerovo, Russia.",{"name":129,"class":107},"Mikhail Vasilev, Meshalkin National Medical Research Center, Мeshalkin of the ministry of health of the Russian Federation,Novosibirsk,Russia.",{"name":131,"class":107},"Jia Min, The First Affiliated Hospital of Nanchang University, Nanchang, China.",{"name":133,"class":107},"Jiawan Wang, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China",{"name":135,"class":107},"Zongbin Song, Xiangya Hospital, Central South University, Changsha, China.","100570077",false,"NCT06702553","Nitric Oxide for Reduced Intensive Support in Cardiac Surgery With Cardiopulmonary Bypass","Effect of Inhaled Nitric Oxide on Major Adverse Events Requiring Intensive Life Support in Adults Undergoing Cardiac Surgery With Cardiopulmonary Bypass: A Phase III, Double-Blind, Multicenter, Randomized Controlled Trial (Nitric Oxide for Reduced Intensive Support in Cardiac Surgery With Cardiopulmonary Bypass, the NORISC Trial)","NORISC","Inclusion Criteria:\n\n1. Age ≥18 years.\n2. Elective cardiac or aortic surgery requiring CPB\n3. Without history of previous open heart surgery.\n\nExclusion Criteria:\n\n1. Immediate emergency cardiac surgery;\n2. Cardiac surgery that requires deep hypothermic circulatory arrest;\n3. Planned cardiac surgery for congenital heart disease repair;\n4. Planned for heart transplatation\n5. Ongoing heart failure or low output syndrome already on intensive support (IABP, ECMO, left ventricular assist device such as impella, mechanical ventilation), left ventricular ejection fraction of \\\u003C 30% or comparable, equivalent preoperative conditions\n6. Already accepted or currently on inhaled NO therapy or inhaled\u002Faerosolized prostacyclin in the week prior to the enrollment;\n7. Endstage kidney disease with estimated glomerular filtration rate (eGFR) \\\u003C 15 ml\u002Fmin or already on renal replacement surgery.\n8. Hemophilia A or B\n9. Other terminal stage of chronic disease with life expectancy less than 1 year per evaluation and adjudication of the attending physicians.","ALL","18 Years",{"count":146,"type":147},3650,"ESTIMATED","INTERVENTIONAL",[150],"PHASE3","Cardiac surgery is a procedure that is commonly performed worldwide. Despite these technological advances, cardiac surgery remains a high-risk surgery. Among post-operative complications, acute kidney injury, respiratory failure, myocardial infarction, and stroke as well as cognitive dysfunction are significant causes of mortality in patients undergoing and following cardiac surgery. Inhaled nitric oxide (NO) therapy as a selective pulmonary vasodilator in cardiac surgery has been one of the most significant pharmacological advances in managing pulmonary hemodynamics and life threatening right ventricular dysfunction and failure. In addition, newer applications show greater promise of inhaled NO as a therapy in the area of cardiac surgery associated acute kidney injury and ischemia reperfusion. However, this remarkable expectation to inhaled NO has experienced a roller-coaster ride with high hopes and nearly universal demonstration of physiological benefits but disappointing translation of these benefits to harder clinical outcomes, like mortality. Most of our understanding on the iNO field in cardiac surgery stems from small observational or single center randomized trials, which failed to ascertain strong evidence base. As a consequence, there are only week clinical practice guidelines on the field and only European expert opinion for the use of iNO in routine and more specialized cardiac surgery. There is need for a large multicenter randomized controlled study to confirm the administration of iNO as an effective weapon for the battle against life threatening complication in high risk cardiac surgical patients.\n\nIn a previous meta analysis with 27 studies included, we demonstrated that inhaled nitric oxide (NO) could reduce the duration of mechanical ventilation and reducing biomarkers of organ injury and clinical signs of organ dysfunction in cardiac surgery under cardiopulmonary bypass (CPB) , but had no significance in the ICU stay, hospital stay, and mortality. This may be attributed to the small sample size of the most included studies (of the 27 studies included, 20 studies with sample size less than 100) and heterogeneity in timing, dosage and duration of iNO administration. Well-designed, large-scale, multicenter clinical trials are needed to further explore the effect of iNO in improving postoperative prognosis in cardiovascular surgical patients.\n\nWe are planning a large multicenter controlled randomized trial to demonstrate that inhaled nitric oxide can reduce composite outcome of death and Major Adverse Events (MAEs), including need for intensive supports due to heart failure, low cardiac output sydrome, or renal failure, respiratory failure, etc., and myocardial infarction, stroke, and sepsis at 30 days after surgery from 20% to 16% in patient undergoing cardiac surgery with cardiopulmonary bypass.\n\nIf the hypothesis had been proved and validated, the results of this study can provide strong evidence for guidelines to facilitate the routine use of iNO in all cardiopulmonary bypass assisted cardiac procedures with 31,800 postoperative outcomes improved per year in US and in China.",[153,154,155,156],"Nitric Oxide","Cardiac Surgery","Cardiopulmonary Bypass","Adult Patients Undergoing Cardiovascular Surgery With Cardiopulmonary Bypass",[153,158,159,160,161,162],"cardiopulmonary bypass","major adverse events","cardiac surgery","complications","Organ protection","2026-05-26",{"date":165,"type":166},"2026-05-29","ACTUAL",{"date":168,"type":166},"2025-05-19",{"date":170,"type":147},"2029-03-31",{"name":5,"class":6},3]