[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Institute of Health Information and Statistics of the Czech Republic\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":303},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,10,0,[8,53,88,115,142,170,194,223,249,278],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":30,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100594112","the-combined-first-trimester-screening-100594112",false,"NCT07015203","The Combined First Trimester Screening","Inclusion Criteria:\n\n* A woman over 18 years old in the first trimester of pregnancy (11th-13th gestational week)\n* Signed the Consent to Participate in the Project and GDPR.\n\nExclusion Criteria:\n\n* Unsigned the Consent to Participate in the Project and the Consent to the Processing of Personal Data.","FEMALE","18 Years",{"count":18,"type":19},2000,"ESTIMATED","OBSERVATIONAL","The project is a national, prospective, multicenter pilot project. The project is focus on setting up the combined first trimester screening in the Czech Republic.\n\nThe combined first trimester screening is aimed at predicting and detecting the most serious obstetric complications, such as the great obstetrical syndromes (preeclampsia, fetal growth restriction, preterm labor and intrauterine fetal demise \"IUFD\") and structural congenital defects (morphological and chromosomal).\n\nThe primary objective of the project is to create a unified methodology for performing and evaluating the combined first trimester screening in connection with the National Health Information System (hereinafter referred to as \"NHIS\"), which will enable recording, providing analysis and linking recorded clinical parameters with data in the NHIS. The pilot project will also provide data for modeling appropriate mechanisms for reimbursement from public health insurance.",[23,24,25,26,27,28,29],"Preeclampsia (PE)","Fetal Growth Restriction","Congenital Abnormalities","Preterm Labor","Intrauterine Fetal Demise","Genetics Syndrome","Pregnancy Overdue - Week 41+6",[31,32,33,34,35,36,37,38,39],"preeclampsia","prediction","prevention","maternal risk factors","Mean Arterial Pressure","Uterine artery Pulsatility Index","Placental Growth Factor","acetylsalicylic acid","Czech Republic","RECRUITING","2026-04-16",{"date":43,"type":44},"2026-04-17","ACTUAL",{"date":46,"type":44},"2025-06-15",{"date":48,"type":19},"2027-04-30",{"name":50,"class":51},"Institute of Health Information and Statistics of the Czech Republic","OTHER_GOV",3,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":60,"minAge":61,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":74,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},"100619847","early-detection-of-skin-tumors-using-a-telemedicine-tool-in-primary-care-100619847","NCT07349940","Early Detection of Skin Tumors Using a Telemedicine Tool in Primary Care","MEL","Inclusion Criteria:\n\n* at least 1 suspected lession\n* phototype I or phototype II\n\nExclusion Criteria:\n\n* skin lession examination by dermatologist in last 12 months\n* unsigned consent to participate in the project and consent to the processing of personal data","ALL","50 Years",{"count":63,"type":19},1440,"INTERVENTIONAL",[66],"NA","The project is a national, prospective, multicenter, single-arm interventional pilot of screening skin tumors in the Czech Republic.\n\nThe primary aim of the project is to methodically prepare, implement and evaluate a pilot project that will verify the suitability of the proposed procedure of early detection of skin tumors by using a telemedicine tools and setting up and testing new methods and implementation into the system of social health care.",[69,70,71,72,73],"Skin Cancer Prevention","Melanoma In Situ","Skin Lesions","Skin Cancer","Mole (Dermatology)",[75,76,77,78],"skin cancer","melanoma","telemedicine tool","skin tumors","2026-03-25",{"date":81,"type":44},"2026-03-27",{"date":83,"type":44},"2026-02-01",{"date":85,"type":19},"2026-09-30",{"name":50,"class":51},5,{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":4,"eligibilityCriteria":94,"healthyVolunteers":11,"sex":60,"minAge":95,"maxAge":95,"enrollmentInfo":96,"targetDuration":4,"studyType":64,"phases":98,"briefSummary":99,"conditions":100,"keywords":102,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":106,"lastUpdatePostDateStruct":107,"startDateStruct":109,"completionDateStruct":111,"leadSponsor":113,"locationsCount":114},"100623045","early-detection-of-developmental-abnormalities-of-preterm-infants-at-5-years-of-age-100623045","NCT07391527","Early Detection of Developmental Abnormalities of Preterm Infants at 5 Years of Age","Early Detection and Prevention of Health Complications in Premature Infants - Early Detection of Developmental Abnormalities of Preterm Infants at 5 Years of Age","Inclusion Criteria:\n\n* Signed consent for participation in the project and consent for the processing of personal data.\n* Children born before 37 weeks of gestation, aged 5 years, growing up in a Czech-speaking environment.\n* To ensure valid linkage of all data sources, the children must have been born to parents with Czech citizenship.\n\nExclusion Criteria:\n\n* Unsigned consent for participation in the project and consent for the processing of personal data.\n* Severe psychomotor retardation .\n* Severe congenital malformations.","5 Years",{"count":97,"type":19},210,[66],"The project is a national, prospective, multicenter, interventional pilot project focused on the follow up of 5 year old children that were born prematurely.\n\nThe primary aim of the project is to prepare, test, and develop a proposal for a national methodology for the care of children born prematurely. This will minimize the negative impacts on the overall development of the child and the family of the prematurely born children.",[101],"5 Year Old Children Born Prematurely",[103,104,105,39],"follow up of premature infants","early detection","developmental abnormality","2026-02-02",{"date":108,"type":44},"2026-02-06",{"date":110,"type":44},"2025-09-23",{"date":112,"type":19},"2027-02-28",{"name":50,"class":51},4,{"id":116,"slug":117,"hasResults":11,"nctId":118,"briefTitle":119,"officialTitle":120,"acronym":4,"eligibilityCriteria":121,"healthyVolunteers":11,"sex":60,"minAge":16,"maxAge":4,"enrollmentInfo":122,"targetDuration":4,"studyType":64,"phases":124,"briefSummary":125,"conditions":126,"keywords":128,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":138,"leadSponsor":140,"locationsCount":141},"100621467","early-detection-of-oab-and-elimination-of-negative-impact-on-quality-of-life-100621467","NCT07371000","Early Detection of OAB and Elimination of Negative Impact on Quality of Life","Early Detection of Overactive Bladder and Elimination of Negative Impact on Quality of Life","Inclusion criteria:\n\n* Signed Consent to Participate in the Project and Consent to the Processing of Personal Data (online and paper format)\n* Men and women over 18 years of age with increased urinary frequency (more than 7 times in 24 hours)\n\nOptional inclusion criteria:\n\n\\- Nycturia and\u002For urge incontinence.\n\nExclusion criteria:\n\n* Unsigned Consent to Participate in the Project and Consent to the Processing of Personal Data.\n* Current treatment of OAB, acute problems, suspicion of another disease causing OAB symptoms (haematuria, suspected bladder cancer, etc.)\n* Inflammation of the lower urinary tract.",{"count":123,"type":19},1000,[66],"Overactive bladder (OAB) is one of the most common health problems in the adult population. The goal of this project is to improve the awareness of the problem and to correctly refer the targeted persons to a specialist or a doctor. This will be provided by an online screening tool, designed as web platform and mobile application, where the data will be stored in respect to GDPR. People with a positive result from the online screening tool will be offered an examination by a specialist (gynaecologist, urogynaecologist, urologist) involved in the project. The specialist will have access to the results from the online screening tool - he\u002Fshe will log into the web platform with a view of the participants profile. He\u002Fshe will perform the diagnosis, confirm or refute the diagnosis and complement it with any further diagnostic tests and set the standard treatment.",[127],"Overactive Bladder (OAB)",[129,130,131,132],"Overactive bladder","Screening","Telemedicine","Online screening tool","2026-01-22",{"date":135,"type":44},"2026-01-27",{"date":137,"type":44},"2025-09-01",{"date":139,"type":19},"2026-08-31",{"name":50,"class":51},20,{"id":143,"slug":144,"hasResults":11,"nctId":145,"briefTitle":146,"officialTitle":147,"acronym":4,"eligibilityCriteria":148,"healthyVolunteers":11,"sex":60,"minAge":149,"maxAge":150,"enrollmentInfo":151,"targetDuration":4,"studyType":64,"phases":153,"briefSummary":154,"conditions":155,"keywords":157,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":169,"locationsCount":87},"100620967","protocol-driven-nutrition-in-preterm-infants-100620967","NCT07364500","Protocol-driven Nutrition in Preterm Infants","Early Detection and Prevention of Health Complications in Premature Infants - Protocol-driven Nutrition","Inclusion Criteria:\n\n* Infants born before 31+6 weeks gestation.\n* Signed consent for participation in the project and consent for the processing of personal data.\n* Admission to neonatal care in the participating hospital within 24 hours after birth.\n\nExclusion Criteria:\n\n* Congenital malformations.\n* Fetal hydrops.\n* Intraventricular hemorrhage requiring drainage.\n* Necrotizing enterocolitis requiring surgical treatment.\n* Surgically treated hydrocephalus.\n* Unsigned consent for participation in the project and\u002For consent for the processing of personal data.","22 Weeks","32 Weeks",{"count":152,"type":19},400,[66],"The project is a national, prospective, multicenter, interventional pilot project focused on protocol-driven nutrition in preterm infants in the Czech republic.\n\nThe primary aim of the project is to prepare, test, and develop a proposal for a national methodology for the care of preterm newborns in the field of nutrition. This will reduce health risks in premature infants and minimize the negative impacts on the overall development of the child and the family of the premature infant.",[156],"Preterm Infants",[158,159,160,161,39],"preterm infants","nutrition of preterm infants","human milk analysis","nutrition monitoring","2026-01-21",{"date":164,"type":44},"2026-01-23",{"date":166,"type":44},"2025-08-21",{"date":168,"type":19},"2027-02",{"name":50,"class":51},{"id":171,"slug":172,"hasResults":11,"nctId":173,"briefTitle":174,"officialTitle":175,"acronym":176,"eligibilityCriteria":177,"healthyVolunteers":11,"sex":60,"minAge":16,"maxAge":4,"enrollmentInfo":178,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":180,"conditions":181,"keywords":183,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":186,"lastUpdatePostDateStruct":187,"startDateStruct":189,"completionDateStruct":191,"leadSponsor":193,"locationsCount":5},"100582593","early-detection-of-cteph-in-patients-after-ape-100582593","NCT06865326","Early Detection of CTEPH in Patients After APE","Early Detection of Chronic Thromboembolic Pulmonary Hypertension in Patients After Acute Pulmonary Embolism","CTEPH","Inclusion Criteria:\n\n* Age over 18 years\n* Signed consent to participate in the project and GDPR\n* Patients with an episode of acute pulmonary embolism in the last 3-12 months, with ongoing anticoagulation therapy:\n\n  1. Patients with new-onset and ongoing or progressive dyspnea (min. NYHA II) after a pulmonary embolism episode or worsening of dyspnea after a pulmonary embolism episode compared to the status before the episode (at least 1 HYHA grade) or\n  2. Asymptomatic patients after a pulmonary embolism episode and at least one of the following risk factors:\n* ECHO evidence of severe PH at diagnosis of PE (PASP \\>60 mmHg)\n* Antiphospholipid syndrome with triple positivity (presence of lupus anticoagulans + anti-beta-2-glycoprotein I (B2GPI) antibodies + anticardiolipin)\n* Infected permanent venous inlets and cardiac pacing\u002Fdefibrillation intravascular systems\n* Presence of ventriculoatrial shunt for treatment of hydrocephalus\n* Nonspecific intestinal inflammation (ulcerative colitis, Crohn's disease)\n* History of splenectomy\n* Myeloproliferative disorders\n* Chronic osteomyelitis\n\nExclusion Criteria:\n\n* Not agreeing to participate in the project\n* Contraindications to treatment",{"count":179,"type":19},500,"The project is a national, prospective, multicenter, observational pilot project of screening CTEPH in pacients after APE in the Czech Republic. The main goal of the project is to methodically prepare, implement and evaluate a pilot project that will verify the suitability of the proposed procedure of early detection of Chronic tromboembolic pulmonary hypertesion in such a way as to ensure the maximum positive impact on the health of the population and high cost-effectiveness of the whole process.",[182],"Chronic Pulmonary Thromboembolism",[176,184,185,39],"APE","Early detection","2025-11-18",{"date":188,"type":44},"2025-11-21",{"date":190,"type":44},"2025-03-07",{"date":192,"type":19},"2026-12-01",{"name":50,"class":51},{"id":195,"slug":196,"hasResults":11,"nctId":197,"briefTitle":198,"officialTitle":199,"acronym":4,"eligibilityCriteria":200,"healthyVolunteers":11,"sex":60,"minAge":4,"maxAge":201,"enrollmentInfo":202,"targetDuration":4,"studyType":64,"phases":204,"briefSummary":205,"conditions":206,"keywords":209,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":222,"locationsCount":114},"100605391","controlled-remote-monitoring-and-optimization-of-oxygen-therapy-in-preterm-infants-100605391","NCT07161908","Controlled Remote Monitoring and Optimization of Oxygen Therapy in Preterm Infants","Early Detection and Prevention of Health Complications in Preterm Infants - Controlled Remote Monitoring and Optimization of Oxygen Therapy","Inclusion Criteria:\n\n* infants born before 31+6 weeks gestation\n* signed consent for participation in the project and consent for the processing of personal data\n* diagnosed with bronchopulmonary dysplasia\n* type of pulmonary ventilation - low-flow nasal cannulas\n\nExclusion Criteria:\n\n* unsigned consent for participation in the project and\u002For consent for the processing of personal data\n* child diagnosed with conditions other than bronchopulmonary dysplasia (BPD) at high risk of long-term hypoxia - selected chronic cardiovascular, neurological, and muscular diseases, e.g., significant congenital heart defects, congenital central nervous system developmental disorders, genetic diseases associated with the risk of hypoventilation, central apneas, severe early obstructive sleep apnea\n* other chronic respiratory diseases besides BPD - e.g., cystic fibrosis, chronic aspiration\n* insufficient therapy through long-term home oxygen therapy\n* tracheostomy","36 Weeks",{"count":203,"type":19},70,[66],"The project is a national, prospective, multicenter, interventional pilot project focused on controlled remote monitoring and optimization of oxygen therapy for premature infants in the Czech Republic. The primary aim of the project is to prepare, test, and develop a proposal for a national methodology for the care of preterm newborns. This will reduce health risks in premature infants and minimize the negative impacts on the overall development of the child and the family of the premature infant.",[207,208],"BPD - Bronchopulmonary Dysplasia","Pulmonary Hypertension",[210,211,158,212,213,214,215,39],"BPD","Bronchopulmonary Dysplasia","oxygen therapy","telemedicine","remote monitoring","pulmonary hypertension","2025-09-04",{"date":218,"type":44},"2025-09-09",{"date":220,"type":44},"2025-08-25",{"date":168,"type":19},{"name":50,"class":51},{"id":224,"slug":225,"hasResults":11,"nctId":226,"briefTitle":227,"officialTitle":227,"acronym":228,"eligibilityCriteria":229,"healthyVolunteers":11,"sex":60,"minAge":230,"maxAge":231,"enrollmentInfo":232,"targetDuration":4,"studyType":64,"phases":233,"briefSummary":234,"conditions":235,"keywords":237,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":240,"lastUpdatePostDateStruct":241,"startDateStruct":243,"completionDateStruct":245,"leadSponsor":247,"locationsCount":248},"100597358","national-childhood-obesity-prevention-programme-be-fit-24-100597358","NCT07057453","National Childhood Obesity Prevention Programme BE FIT 24","BE FIT 24","Inclusion Criteria:\n\n* Age: 6-11 years\n* BMI: Between the 90th and 97th percentile\n* Signed consent to participate in the project and GDPR\n\nExclusion Criteria:\n\n* Children with a BMI between the 90th and 97th percentile with an associated chronic disease requiring continuous pharmacological treatment","6 Years","11 Years",{"count":123,"type":19},[66],"The project is a national, prospective, multicenter, interventional pilot project of early detection of childhood overweight and the prevention of obesity in the Czech Republic.\n\nThe main goal of the project is to methodically prepare, implement and evaluate a pilot project that will verify the suitability of the proposed procedure of early detection of childhood overweight and the prevention of obesity and setting up and testing new methods and implementation into the system of health care.",[236],"Childhood Obesity",[185,238,239],"Overweight","Fitness bracelets","2025-07-04",{"date":242,"type":44},"2025-07-09",{"date":244,"type":44},"2024-11-19",{"date":246,"type":19},"2026-12-31",{"name":50,"class":51},1,{"id":250,"slug":251,"hasResults":11,"nctId":252,"briefTitle":253,"officialTitle":254,"acronym":255,"eligibilityCriteria":256,"healthyVolunteers":11,"sex":60,"minAge":16,"maxAge":4,"enrollmentInfo":257,"targetDuration":259,"studyType":20,"phases":4,"briefSummary":260,"conditions":261,"keywords":263,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":269,"lastUpdatePostDateStruct":270,"startDateStruct":272,"completionDateStruct":274,"leadSponsor":276,"locationsCount":277},"100549279","early-detection-of-hcv-in-injection-drug-users-100549279","NCT06431945","Early Detection of HCV in Injection Drug Users","Early Detection of Hepatitis C in Injection Drug Users","EDVIP","Inclusion Criteria:\n\n* age 18+\n* an active injecting drug user or have used injecting drugs at any time in the past\n\nExclusion Criteria:\n\n* not agreeing to participate in the project",{"count":258,"type":19},3000,"2 Months","The project is a national, prospective, multicenter, non-interventional pilot project of screening HCV in PWID in the Czech Republic.\n\nThe main goal of the project is to methodically prepare, implement and evaluate a pilot project that will verify the suitability of the proposed procedure of early detection of Hepatitis C and setting up and testing new methods and implementation into the system of social health care.",[262],"Hepatitis C Virus Infection",[264,265,266,267,39,268],"HCV","PWID","Point of care testing","Hepatitis","HCV genotype","2025-06-25",{"date":271,"type":44},"2025-06-29",{"date":273,"type":44},"2023-12-15",{"date":275,"type":19},"2025-12-31",{"name":50,"class":51},18,{"id":279,"slug":280,"hasResults":11,"nctId":281,"briefTitle":282,"officialTitle":283,"acronym":284,"eligibilityCriteria":285,"healthyVolunteers":11,"sex":60,"minAge":16,"maxAge":4,"enrollmentInfo":286,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":287,"conditions":288,"keywords":290,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":294,"lastUpdatePostDateStruct":295,"startDateStruct":297,"completionDateStruct":299,"leadSponsor":301,"locationsCount":302},"100554479","early-detection-of-malnutrition-in-oncology-patients-and-elderly-patients-100554479","NCT06499623","Early Detection of Malnutrition in Oncology Patients and Elderly Patients","Early Detection of Malnutrition in Oncology Patients and People Over 65 Years of Age","MALNUTRITION","Inclusion Criteria:\n\nCohort Oncological patients:\n\n* 18+\n* an oncological diagnosis\n* a survival prognosis of at least 3 months\n\nCohort Patients older than 65 years:\n\n* 65+\n* hospitalization at least 14 days or longer\n\nExclusion Criteria (both cohorts):\n\n* not agreeing to participate in the project",{"count":18,"type":19},"The project is a national, prospective, multicenter, non-interventional pilot project of malnutrition screening in the Czech Republic.\n\nThe main goal of the project is to methodically prepare, implement and evaluate a pilot project that will verify the suitability of the proposed procedure for the early detection of malnutrition in oncology patients and hospitalised patients patients 65 years of age and older, as this has a significant effect on the quality of life and the effectiveness of the services provided oncological treatment.",[289],"Malnutrition",[291,292,293],"malnutrition","oncology","gerontology","2024-10-01",{"date":296,"type":44},"2024-10-03",{"date":298,"type":44},"2024-08-29",{"date":300,"type":19},"2026-03-31",{"name":50,"class":51},9,""]