[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100538459":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":29,"locations":35,"responsibleParty":103,"collaborators":25,"id":105,"slug":106,"hasResults":107,"nctId":108,"briefTitle":109,"officialTitle":109,"acronym":110,"eligibilityCriteria":111,"healthyVolunteers":107,"sex":112,"minAge":113,"maxAge":114,"enrollmentInfo":115,"targetDuration":25,"studyType":118,"phases":119,"briefSummary":121,"conditions":122,"keywords":25,"overallStatus":38,"whyStopped":25,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":133},{"fullName":5,"class":6},"University Hospital, Rouen","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"experimental","EXPERIMENTAL","Experimental group: standard care + rotigotine at 4 mg\u002F24 hours for 24 months.",[13],"Drug: standard care + rotigotine at 4 mg\u002F24h for 24 months.",{"label":15,"type":16,"description":17,"interventionNames":18},"Control","ACTIVE_COMPARATOR","Control group: standard care for 24 months.",[19],"Drug: standard care for 24 months.",[21,26],{"type":22,"name":23,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","standard care + rotigotine at 4 mg\u002F24h for 24 months.",[9],null,{"type":22,"name":27,"description":27,"armGroupLabels":28,"otherNames":25},"standard care for 24 months.",[15],[30],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},"Dominique Guerrot, Pr","CONTACT","02 32 88 54 46","Dominique.Guerrot@chu-rouen.fr",[36,56,71,86],{"facility":37,"status":38,"city":39,"state":25,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"CHU d'AMIENS","RECRUITING","Amiens","80054","France","FR",{"type":44,"coordinates":45},"Point",[46,47],2.3,49.9,{"lat":47,"lon":46},[50,54],{"name":51,"role":32,"phone":52,"phoneExt":25,"email":53},"Gabriel Choukroun, Dr","03 22 45 54 62","choukroun.gabriel@chu-amiens.fr",{"name":51,"role":55,"phone":25,"phoneExt":25,"email":25},"PRINCIPAL_INVESTIGATOR",{"facility":57,"status":38,"city":58,"state":25,"zip":59,"country":41,"countryCode":42,"cosmosGeoPoint":60,"geoPoint":64,"contacts":65},"CHRU de CAEN","Caen","14033",{"type":44,"coordinates":61},[62,63],-0.35912,49.18585,{"lat":63,"lon":62},[66,70],{"name":67,"role":32,"phone":68,"phoneExt":25,"email":69},"Clémence Bechade, Dr","02 31 27 25 76","bechade-c@chu-caen.fr",{"name":67,"role":55,"phone":25,"phoneExt":25,"email":25},{"facility":72,"status":38,"city":73,"state":25,"zip":74,"country":41,"countryCode":42,"cosmosGeoPoint":75,"geoPoint":79,"contacts":80},"CHU de LILLE","Lille","59037",{"type":44,"coordinates":76},[77,78],3.05512,50.63391,{"lat":78,"lon":77},[81,85],{"name":82,"role":32,"phone":83,"phoneExt":25,"email":84},"François-Xavier Glowacki, Dr","03 20 44 40 75","Francois.GLOWACKI@CHRU-LILLE.FR",{"name":82,"role":55,"phone":25,"phoneExt":25,"email":25},{"facility":87,"status":38,"city":88,"state":25,"zip":89,"country":41,"countryCode":42,"cosmosGeoPoint":90,"geoPoint":94,"contacts":95},"CHU de ROUEN","Rouen","76031",{"type":44,"coordinates":91},[92,93],1.09932,49.44313,{"lat":93,"lon":92},[96,99,100],{"name":31,"role":32,"phone":97,"phoneExt":25,"email":98},"02.32.88.31.21","Audrey.Dumont@chu-rouen.fr",{"name":31,"role":55,"phone":25,"phoneExt":25,"email":25},{"name":101,"role":102,"phone":25,"phoneExt":25,"email":25},"Audrey Dumont, Dr","SUB_INVESTIGATOR",{"type":104,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR","100538459","phase-2-safety-of-rotigotine-in-patients-with-autosomal-dominant-polycystic-kidney-disease-100538459",false,"NCT06291116","Safety of RotigotiNe in Patients With Autosomal Dominant Polycystic Kidney Disease","ETERNAL-PKD","Inclusion Criteria:\n\n* ADPKD patients aged 18 to 60 years\n* Normotensive or hypertensive patients treated controlled (SBP\u002FDBP on daytime ABPM \\\u003C135\u002F85 mmHg less than 3 months old)\n* Patient having read and understood the information letter and signed the consent form\n* Effective contraception in women of childbearing age (for postmenopausal women, a confirmatory diagnosis should be obtained)\n* Patient benefiting from a social protection scheme\n\nExclusion Criteria:\n\n* Stage 4 or 5 renal insufficiency (GFR CKD-EPI \\\u003C30 ml\u002Fmin)\n* Renal transplant patients\n* Dialysis patients\n* History of myocardial infarction or stroke less than 6 months old\n* Severe hepatic insufficiency (Child-Pugh class C)\n* Patients currently being treated or treated in the 6 months preceding the trial with a dopamine agonist or antagonist\n* Systolic heart failure requiring hospitalization in the 6 months preceding inclusion or known heart failure with an LVEF \\\u003C30%\n* Orthostatic hypotension (decrease \\> 20 mm Hg)\n* Pregnant, breastfeeding woman, or proven absence of contraception\n* Excessive alcohol consumption (greater than 20 g\u002Fday)\n* History of addictive behavior, particularly gambling, compulsive purchasing or hypersexuality\n* Drug addiction or suspected illicit drug use\n* Taking other sedative medications or other central nervous system depressants (benzodiazepines, antipsychotics, antidepressants or neuroleptics with antiemetic intent)\n* Hypersensitivity to the active ingredient, rotigotine, or to one of its excipients\n* Known allergy to sulphites\n* Person deprived of liberty by an administrative or judicial decision or person placed under judicial protection, or guardianship or curatorship.","ALL","18 Years","60 Years",{"count":116,"type":117},120,"ESTIMATED","INTERVENTIONAL",[120],"PHASE2","Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is caused by mutations in the PKD1 or PKD2 genes, which encode polycystins 1 and 2. Patients develop renal cysts associated with a progressive decline in kidney function, ultimately leading to end-stage renal disease in approximately one third of cases. ADPKD is also characterized by early-onset hypertension and cardiovascular complications, notably intracranial aneurysms.\n\nThis phenotype is related to abnormal polycystin function in the primary cilia of renal epithelial and vascular endothelial cells, resulting in impaired mechanotransduction of shear stress induced by urinary and blood flow and subsequent alterations in multiple cellular functions. Experimental studies have suggested that stimulation of dopamine receptor type 5 (DR5) may restore endothelial mechanosensitivity. This hypothesis is supported by our preliminary results showing that local administration of dopamine improves endothelial function in patients with ADPKD through restoration of nitric oxide (NO) release in response to increased blood flow.\n\nConsistent with these findings, the IMPROVE-PKD study recently demonstrated similar beneficial effects on endothelial function and hemodynamics using rotigotine, a dopamine agonist administered via transdermal patches for two months at a low dose (4 mg\u002F24 h). Dopaminergic stimulation may also prevent renal abnormalities related to polycystin deficiency. We therefore hypothesize that rotigotine could slow the progression of ADPKD at both the renal and cardiovascular levels.\n\nThis phase 2 study aims to evaluate the long-term tolerability of rotigotine in patients with ADPKD and to collect preliminary data on its effects on renal outcomes.",[123],"Kidney Diseases","2026-06-05",{"date":126,"type":127},"2026-06-09","ACTUAL",{"date":129,"type":127},"2026-05-12",{"date":131,"type":117},"2030-07-01",{"name":5,"class":6},4]