[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hemodialysis-patients\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hemodialysis-patients":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,55,90,116,143,173,198],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":31,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100644867","euvolemia-based-assessment-of-pulmonary-hypertension-in-stable-hemodialysis-patients-100644867",false,"NCT07676786","Euvolemia-Based Assessment of Pulmonary Hypertension in Stable Hemodialysis Patients","Prospective Observational Study on Predictors and Types of Pulmonary Hypertension in Euvolemic Patients With End-Stage Kidney Disease on Maintenance Hemodialysis","EU-PHASE-HD","Inclusion Criteria:\n\n* Age ≥ 18 years.\n* End-stage kidney disease on maintenance HD for ≥ 3 months.\n* Stable clinical condition (no hospitalization in last 30 days).\n* Able and willing to comply with study protocol.\n* Provision of written informed consent\n\nExclusion Criteria:\n\n* Moderate\u002Fsevere left-sided valvular disease.\n* Active pulmonary or cardiac decompensation.\n* Persistent hypervolemia after completion of the volume assessment and correction phase\n* Inability to undergo echocardiography or bioimpedance assessment.\n* Acute infection or inflammatory condition at the time of enrollment.\n* Inadequate echocardiographic window preventing reliable assessment","ALL","18 Years",{"count":20,"type":21},30,"ESTIMATED","OBSERVATIONAL","Pulmonary hypertension (PH) is a frequent and clinically significant complication in patients with end-stage kidney disease (ESKD) undergoing maintenance hemodialysis (HD). However, PH assessment in this population is often confounded by volume overload, leading to potential overestimation and misclassification.\n\nThis prospective, multicenter observational study aims to evaluate the prevalence, phenotype, and predictors of PH in HD patients under standardized euvolemic conditions. A structured pretrial phase including volume assessment and correction will be performed prior to echocardiographic evaluation, which will be conducted after confirmation of euvolemia, post-hemodialysis or on the following day.\n\nIn participants with echocardiographic findings suggestive of PH, right heart catheterization may be performed when clinically indicated and after obtaining specific informed consent.\n\nThe study integrates clinical, biological, dialysis-related, and echocardiographic data to provide a comprehensive characterization of PH in a well-defined ESKD population.",[25,26,27,28,29,30],"Pulmonary Hypertension (PH)","End Stage Kidney Disease (ESRD)","Hemodialysis Patients","Volume Overload","Volume Assessment","Hemodialysis",[32,30,33,34,28,35,36,37,38,39,40,41],"Pulmonary Hypertension","End-Stage Kidney Disease","Euvolemia","Volume Status","Echocardiography","Bioimpedance Spectroscopy","Interdialytic Weight Gain","Vascular Access","Blood Pressure Variability","Lung Ultrasound","NOT_YET_RECRUITING","2026-06-24",{"date":45,"type":46},"2026-06-30","ACTUAL",{"date":48,"type":21},"2026-07-01",{"date":50,"type":21},"2027-03-30",{"name":52,"class":53},"Stefan Lujinschi","OTHER",2,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":61,"eligibilityCriteria":62,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":63,"targetDuration":4,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":72,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":89},"100606757","using-a-hypotension-prediction-index-to-prevent-low-blood-pressure-during-dialysis-in-icu-patients-100606757","NCT07179705","Using a Hypotension Prediction Index to Prevent Low Blood Pressure During Dialysis in ICU Patients","Hypotension Prediction Index Guided Prevention of Intradialytic Hypotension During Intermittent Renal Replacement Therapy in Intensive Care Units","HyPIR-ICU","Inclusion Criteria:\n\n* Adults \\>18 years old\n* Diagnosed with acute kidney injury (AKI) or end-stage kidney disease (ESKD)\n* Admitted to medical ICU\n* Scheduled for PIRRT\n* Have an indwelling arterial catheter\n\nExclusion Criteria:\n\n* Severe right heart dysfunction, significant valvular disease, arrhythmias, mechanical circulatory support, absence of arterial access, no UF prescription, palliative care, or expected ICU stay \\\u003C72 hours.",{"count":64,"type":21},46,"INTERVENTIONAL",[67],"NA","This single-center, crossover randomized controlled trial (HyPIR-ICU) investigates whether a Hypotension Prediction Index (HPI)-guided management strategy can reduce intradialytic hypotension (IDH) during prolonged intermittent renal replacement therapy (PIRRT) in critically ill patients. All participants must have an indwelling arterial catheter for continuous hemodynamic monitoring.",[70,71,27],"Intradialytic Hypotension","Intensive Care Unit ICU",[73,74,75,76,77,78],"Hypotension Prediction Index (HPI)","Prolonged intermittent renal replacement therapy (PIRRT)","Slow-low efficiency dialysis","Intradialytic hypotension","Hemodynamic monitoring","Intensive Care Unit","RECRUITING","2026-05-05",{"date":82,"type":46},"2026-05-07",{"date":84,"type":46},"2025-10-10",{"date":86,"type":21},"2026-12-31",{"name":88,"class":53},"Chulalongkorn University",1,{"id":91,"slug":92,"hasResults":11,"nctId":93,"briefTitle":94,"officialTitle":94,"acronym":4,"eligibilityCriteria":95,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":96,"targetDuration":4,"studyType":65,"phases":98,"briefSummary":99,"conditions":100,"keywords":101,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":4},"100624498","the-effect-of-joint-range-of-motion-and-benson-relaxation-exercises-on-dialysis-adequacy-treatment-adherence-and-quality-of-life-in-hemodialysis-patients-100624498","NCT07410416","The Effect of Joint Range of Motion and Benson Relaxation Exercises on Dialysis Adequacy, Treatment Adherence, and Quality of Life in Hemodialysis Patients","Inclusion Criteria:\n\n* Being 18 years of age or older\n* Receiving HD treatment for at least 1 year\n* Receiving HD treatment 3 days a week for 4 hours\n* Being able to speak Turkish\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Patients with chronic diseases affecting breathing (advanced COPD, cancer)\n* Patients with hearing or speech problems\n* Patients with a diagnosed psychiatric condition\n* Patients with conditions that impede movement, such as burns, open wounds, edema, thrombophlebitis, limited mobility, fistulas, or previous surgical operations in the extremities\n\nExclusion Criteria from the Study:\n\n* Patients whose HD center changed during the study\n* Patients who did not wish to continue with the study\n* Patients who received a diagnosis of neurological or psychiatric illness during the study.",{"count":97,"type":21},72,[67],"The aim of this study is to determine the effects of range of motion and Benson relaxation exercises applied to patients undergoing hemodialysis treatment on dialysis adequacy, treatment adherence, and quality of life.",[27],[30,102,103,104,105,106],"range of motion","Benson relaxation exercises","quality of life","dialysis adequacy","treatment adherence","2026-02-08",{"date":109,"type":46},"2026-02-13",{"date":111,"type":21},"2026-03-01",{"date":113,"type":21},"2026-05-16",{"name":115,"class":53},"Ardahan University",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":122,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":17,"minAge":124,"maxAge":125,"enrollmentInfo":126,"targetDuration":4,"studyType":65,"phases":127,"briefSummary":128,"conditions":129,"keywords":4,"overallStatus":79,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":138,"leadSponsor":140,"locationsCount":89},"100620709","a-comparative-study-of-intradialytic-vs-pre-dialysis-physical-therapy-interventions-in-individuals-undergoing-hemodialysis-a-randomized-controlled-trial-100620709","NCT07361146","A Comparative Study of Intradialytic vs. Pre-Dialysis Physical Therapy Interventions in Individuals Undergoing Hemodialysis: A Randomized Controlled Trial","A Comparative Study of Intradialytic Versus Pre-Dialysis Physical Therapy Interventions in Individuals Undergoing Hemodialysis: A Randomized Controlled Trial","DIAL-PT","Inclusion Criteria:\n\n* Adults aged between 21 and 65 years.\n* Diagnosed with end-stage renal disease (ESRD).\n* Undergoing maintenance hemodialysis for at least 3 months.\n* Medically stable and cleared by the nephrologist to participate in moderate physical exercise.\n* Able to understand and follow verbal instructions and provide informed consent.\n\nExclusion Criteria:\n\n* Uncontrolled hypertension, recent myocardial infarction, or unstable angina.\n* Severe musculoskeletal, neurological, or cardiovascular disorders that limit physical activity.\n* Active infection, fever, or open wounds.\n* Recent hospitalization within the past month.\n* Participation in any other structured exercise program within the last 3 months.","21 Years","65 Years",{"count":97,"type":21},[67],"This randomized controlled trial aims to compare the effectiveness of two different timings of physical therapy for individuals undergoing hemodialysis: intradialytic (during dialysis) and pre-dialysis (before dialysis). The study seeks to determine which approach provides better improvements in physical function, quality of life, and biochemical outcomes such as hemoglobin and electrolyte levels.\n\nA total of 72 adult participants with end-stage renal disease (ESRD) receiving hemodialysis will be randomly assigned to one of two groups. Both groups will receive standardized educational sessions on the benefits and safety of exercise before beginning the intervention. Participants in the intradialytic group will perform supervised exercises during their dialysis sessions, while those in the pre-dialysis group will complete similar exercises before their dialysis sessions. Each participant will undergo the intervention twice per week for 12 weeks.\n\nPrimary outcomes include physical function, assessed using the Six-Minute Walk Test and the Five Times Sit-to-Stand Test. Secondary outcomes include hemoglobin levels, electrolyte balance, and health-related quality of life measured by the KDQOL questionnaire. The study will be conducted at Mubarak Al-Abdullah Al-Jaber Al-Sabah Dialysis Center, Kuwait, following ethical approval from the Ministry of Health Research Ethics Committee.\n\nThe results are expected to inform best practices for integrating physical therapy into dialysis care to enhance the health, safety, and well-being of individuals undergoing hemodialysis.",[130,131,27,132],"End-stage Renal Disease (ESRD)","Chronic Kidney Disease","Physical Rehabilitation During Dialysis","2026-01-14",{"date":135,"type":46},"2026-01-22",{"date":137,"type":46},"2025-03-02",{"date":139,"type":21},"2027-06-02",{"name":141,"class":142},"Mohammad Arian","OTHER_GOV",{"id":144,"slug":145,"hasResults":11,"nctId":146,"briefTitle":147,"officialTitle":148,"acronym":4,"eligibilityCriteria":149,"healthyVolunteers":150,"sex":17,"minAge":18,"maxAge":151,"enrollmentInfo":152,"targetDuration":4,"studyType":65,"phases":154,"briefSummary":155,"conditions":156,"keywords":158,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":164,"lastUpdatePostDateStruct":165,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":89},"100597658","effect-of-therapeutic-touch-on-perceived-stress-and-comfort-levels-in-hemodialysis-patients-100597658","NCT07061353","Effect of Therapeutic Touch on Perceived Stress and Comfort Levels in Hemodialysis Patients","Effect of Therapeutic Touch on Perceived Stress and Comfort Levels in Hemodialysis Patients: A Randomized Controlled Trial","Inclusion Criteria:\n\n* At least 3 months of hemodialysis treatment • Cognitive function is in place\n\nExclusion Criteria:\n\n* Those with communication problems\n* Those who do not agree to participate in the study\n* Patients who receive traditional treatment for the disease",true,"75 Years",{"count":153,"type":21},60,[67],"Hemodialysis is a treatment method used in the treatment of acute or chronic renal failure, the main function of which is based on the cleaning of accumulated waste materials in the blood, and is rapidly developing and spreading in parallel with today's technology. Patients undergoing hemodialysis treatment are trying to cope with social and physical problems that may develop due to chronic disease. At the same time, their quality of life is affected due to the psychosocial, economic problems and complications brought about by machine dependency. From past to present, individuals have used various methods to protect\u002Fimprove their health. Today, in addition to modern medicine, complementary\u002Falternative therapies are increasingly used. One of these alternative therapies is the therapeutic touch application, which has recently gained popularity. Therapeutic touch is based on the therapeutic effect of the act of touching. Therapeutic touch, alternatively known as healing touch, is a complementary\u002Falternative treatment method applied by touching energy points in the body. Therefore, this study was planned to examine the effect of therapeutic touch applied to hemodialysis patients on perceived stress and comfort levels. This study, planned as a randomized experimental study with a pre-test-post-test intervention control group, will be a study on dialysis patients receiving treatment at the hemodialysis unit of Fırat University Hospital between June 2025-June 2026. The sample will consist of a minimum of 60 dialysis patients (30 intervention, 30 control) who meet the research criteria and accept the study. The patients in the intervention and control groups will first be informed about the application before starting the application and their verbal and written consents will be obtained. Then, the Patient Identification Form, Visual Analog Scale-Comfort (VAS-Comfort), Hemodialysis Comfort Scale (HKS) and Perceived Stress Scale (PSS) will be applied and the 1st measurement will be obtained. The application will last approximately 15-30 minutes for the patients in the intervention group every three days. After three days of alternate application, data forms will be filled in again for patients and 2nd measurements will be obtained. During this period, no intervention will be made to patients in the control group and only the normal treatment protocol will be applied. At the end of three days, data forms will be filled in again and 2nd measurements will be obtained. In the analysis of data; frequency and percentage analyses, chi-square analysis, standard deviation, t-test in dependent groups, t-test analysis in independent groups will be performed.",[157,27],"Therapeutic Touch",[159,160,161,162,163],"Therapeutic touch","Hemodialysis Patient","Stress","Comfort","Nursing","2025-11-14",{"date":166,"type":46},"2025-11-18",{"date":168,"type":21},"2025-12-31",{"date":170,"type":21},"2026-06-01",{"name":172,"class":53},"Firat University",{"id":174,"slug":175,"hasResults":11,"nctId":176,"briefTitle":177,"officialTitle":177,"acronym":4,"eligibilityCriteria":178,"healthyVolunteers":150,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":179,"targetDuration":181,"studyType":22,"phases":4,"briefSummary":182,"conditions":183,"keywords":186,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":4},"100606848","study-of-diastolic-dysfunction-in-eskd-in-hemodialysis-patient-100606848","NCT07180888","Study of Diastolic Dysfunction in ESKD in Hemodialysis Patient","Inclusion Criteria:\n\n* age between 18 and 65 years not diagnosed by MI able and willing to provide informed consent\n\nExclusion Criteria:\n\nprevious MI arrythmia CHF\n\n\\-",{"count":180,"type":21},100,"6 Months","To Asses the prevalence , pattern , and severity of diastolic dysfunction in patients ESKD undergoing regular dialysis and to investigate its correlation with clinical parameters dialysis-related factors and echocardiographic findings",[184,185,27],"Heart Failure","ESKD",[187,188],"echocardiography","dialysis patients","2025-09-12",{"date":191,"type":46},"2025-09-18",{"date":193,"type":21},"2025-09-22",{"date":195,"type":21},"2025-10-15",{"name":197,"class":53},"Sohag University",{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":4,"eligibilityCriteria":204,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":125,"enrollmentInfo":205,"targetDuration":4,"studyType":65,"phases":207,"briefSummary":208,"conditions":209,"keywords":210,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":215,"lastUpdatePostDateStruct":216,"startDateStruct":218,"completionDateStruct":220,"leadSponsor":222,"locationsCount":4},"100550594","the-effect-of-mindfulness-compassionate-living-practice-on-hemodialysis-patients-100550594","NCT06449105","The Effect of Mindfulness Compassionate Living Practice on Hemodialysis Patients","The Effect of Mindfulness Compassionate Life Practice on Stress, Self-Efficacy and Quality of Life in Hemodialysis Patients: A Randomized Controlled Study","Inclusion Criteria:\n\n* Being diagnosed with chronic renal failure\n* Being over 18 years of age,\n* Being willing to participate in the study\n* Being open to communication and collaboration\n\nExclusion Criteria:\n\n* Having a diagnosis of acute renal failure,\n* Having a current hospital stay,\n* Lack of openness to communication and collaboration,",{"count":206,"type":21},68,[67],"There are studies evaluating the effects of mindfulness-based practices on individuals receiving HD treatment. No studies have been found on how Mindfulness Compassionate Life application reduces stress, increases self-efficacy and quality of life in individuals receiving HD treatment. Considering the stress situations experienced by individuals receiving HD treatment, it is thought that the evidence-based effect of Mindfulness Compassionate Living application on individuals\\' stress, self-efficacy and quality of life is important.\n\nThe population of the research will consist of 90 Hemodialysis patients who were treated in Bingöl State Hospital Dialysis Unit during the specified date range. Sample size of the research; Calculated using the GPower computer program. With the power analysis, it was calculated that at the α = 0.05 level, the effect size would be strong 150, 153 (d = 0.8) and the power of the study would be 90%, and that at least 68 patients should be included in the sample. Patients who meet the research criteria and agree to participate in the research will be randomly assigned to one experimental and one control group.",[27],[211,212,213,214],"Hemodialysis patients","Mindfulness","Life quality","Self-Efficacy","2024-06-03",{"date":217,"type":46},"2024-06-07",{"date":219,"type":21},"2024-06-15",{"date":221,"type":21},"2024-11-15",{"name":223,"class":53},"Ataturk University"]