[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"renal-denervation\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:renal-denervation":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100601766","renal-denervation-after-stroke-reds-study---a-randomized-clinical-trial-of-renal-denervation-in-the-subacute-phase-of-stroke-100601766",false,"NCT07114757","REnal Denervation After Stroke (REDs) Study - A Randomized Clinical Trial of Renal Denervation in the Subacute Phase of Stroke","REDs","Inclusion Criteria:\n\n\\- We will enroll patients (at least 18 years of age and younger than 85 years old) with subacute stroke (thus occurring 7-45 days before screening), admitted to hospital, with persistently high systolic PB (≥140 mm Hg computed as the mean of 3 repeated measurements taken within 5 minutes between 8.00am and 8.30 am on 2 consecutive days, thus totaling 6 measurements), or a non-dipper profile at ambulatory BP monitoring, despite therapy with ≥2 anti-hypertensive drugs at maximum tolerated dose. Patients should be medically stable with no severe complications such as infections, or worsening of neurological status that would require immediate and intensive medical or surgical intervention.\n\nExclusion Criteria:\n\n* ⦁ Patients with cerebral bleeding due to arteriovenous malformation or intracranial aneurysm\n\n  * Hemodynamic instability\n  * Comorbidity with life expectancy ≤ 1 year\n  * Renal artery anatomy, which prevents the procedure\n  * Reno vascular disease\n  * Vascular occlusion, which prevents the procedure\n  * Secondary hypertension\n  * Subject has known hypersensitivity or contraindication to any of the study drugs\n  * The subject is currently participating in another investigational drug or device clinical study\n  * Pregnancy or nursing\n  * Presence of other anatomic or comorbid conditions or other medical, social, or psychological conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical investigation or to comply with follow-up requirements or impact the scientific soundness of the clinical investigation results","ALL","18 Years","84 Years",{"count":20,"type":21},108,"ESTIMATED","INTERVENTIONAL",[24],"NA","The REnal Denervation after stroke (REDs) study is a national, multicenter, investigator-initiated randomized controlled clinical trial designed to assess the efficacy of catheter-based renal denervation (RDN) performed in the subacute phase of stroke among patients with drug-resistant hypertension. Conducted across 15 Italian centers, this pragmatic trial adopts a parallel-group design with participants randomized in a 1:1 ratio to receive either RDN using the Symplicity Spyral system or standard care. Randomization will occur via a secure online platform, and the intervention will be performed within 24 hours post-randomization, adhering to a standardized procedural protocol.\n\nThe trial targets adult patients aged 18 to 84 years who have experienced a stroke 7 to 45 days prior to enrollment and present with persistent systolic hypertension (≥140 mmHg) or a non-dipping profile on ambulatory blood pressure monitoring, despite the use of at least two antihypertensive medications at maximum tolerated doses. Following informed consent and verification of eligibility, enrolled patients will undergo baseline assessments including physical examination, laboratory testing, ECG, stroke severity and disability scoring, and quality of life evaluation.\n\nThe total duration of the REDs study is 48 months, encompassing a 24-month enrollment window and a 24-month follow-up period. Study endpoints, including 24-hour ambulatory blood pressure and secondary clinical and functional outcomes, will be evaluated at 3, 6, 9, 12, and 24 months following the intervention. These follow-up assessments will be conducted through hospital visits or teleconsultations as appropriate.\n\nThe primary efficacy endpoint is the change in mean 24-hour systolic blood pressure 12 months after randomization. Secondary endpoints include diastolic and mean arterial pressure, antihypertensive medication burden, time to blood pressure control, functional neurological scores (NIHSS, mRS), quality of life metrics, and stroke recurrence. Data collection will be managed via an electronic case report form (eCRF), and adverse events will be monitored throughout the study in line with ISO14155 and GCP standards.\n\nThis trial is supported by an unrestricted grant from Medtronic and adheres to ethical guidelines as outlined by the Declaration of Helsinki and GDPR. The REDs study aims to generate clinically relevant evidence to support the integration of RDN into secondary prevention strategies for stroke patients with resistant hypertension.",[27,28,29,30,31,32],"Cardiovascular Diseases","Cerebrovascular Disease","Arterial Hypertension","Hypertension","Renal Denervation","Stroke","NOT_YET_RECRUITING","2025-08-04",{"date":36,"type":37},"2025-08-11","ACTUAL",{"date":39,"type":21},"2025-09-25",{"date":41,"type":21},"2029-09-25",{"name":43,"class":44},"Centro per la Lotta Contro l'Infarto - Fondazione Onlus","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":22,"phases":58,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":62,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":45},"100494247","renal-denervation-in-patients-with-chronic-heart-failure-with-preserved-ejection-fraction-100494247","NCT05715697","Renal Denervation in Patients With Chronic Heart Failure With Preserved Ejection Fraction","The First Affiliated Hospital of Xinjiang Medical University","RDN-HFPEF","Inclusion Criteria:\n\n1. signs or symptoms of heart failure;\n2. normal or mildly abnormal systolic LV function (LVEF ≥ 50%);\n3. evidence of diastolic LV dysfunction.\n4. Individual should fulfill the diagnostic WHO criteria for hypertension: SBP \\> 140 mmHg and\u002For DBP \\> 90 mmHg, and is treated with at least 2 antihypertensive drugs. This treatment is expected to be maintained for at least 6 months. Using this regimen the blood pressure should be adequately controlled (\\\u003C 140\u002F90mmHg by 24 hour ambulatory BP measurement).\n5. Individual is adhering to a stable drug regimen HFNEF, with no changes for a minimum of 2 weeks prior to enrollment, and which is expected to be maintained for at least 6 months.\n\nExclusion Criteria:\n\n1. Known secondary cause of hypertension\n2. Anatomy not eligible for renal denervation\n3. Systolic heart failure (LVEF \\\u003C 50%)\n4. Individual has an estimated glomerular filtration rate (eGFR) of \\\u003C 30mL\u002Fmin\u002F1.73m2, using the MDRD calculation.\n5. Individual has any serious medical condition, which in the opinion of the investigator, may adversely affect the safety and\u002For effectiveness of the participant or the study (i.e., patients with clinically significant peripheral vascular disease, abdominal aortic aneurysm, bleeding disorders such as thrombocytopenia, haemophilia, significant anaemia, or arrhythmias such as atrial fibrillation).\n6. Individual is pregnant, nursing or planning to be pregnant.","21 Years","80 Years",{"count":57,"type":21},200,[24],"This study aims to explore the potential of RDN as a therapy for HFpEF in a Prospective, Multicenter, Randomized, Blinded, Sham-controlled Study.",[61,31],"Heart Failure With Preserved Ejection Fraction","RECRUITING","2024-01-30",{"date":65,"type":37},"2024-02-01",{"date":67,"type":37},"2023-09-01",{"date":69,"type":21},"2026-09-01",{"name":71,"class":44},"Xinjiang Medical University"]