[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100276617":3},{"organization":4,"outcomesModule":7,"designInfo":22,"detailedDescription":25,"studyPopulation":26,"armGroups":21,"interventions":27,"overallOfficials":31,"centralContacts":36,"locations":42,"responsibleParty":391,"collaborators":21,"id":393,"slug":394,"hasResults":395,"nctId":396,"briefTitle":397,"officialTitle":398,"acronym":21,"eligibilityCriteria":399,"healthyVolunteers":395,"sex":400,"minAge":21,"maxAge":21,"enrollmentInfo":401,"targetDuration":404,"studyType":405,"phases":21,"briefSummary":406,"conditions":407,"keywords":21,"overallStatus":64,"whyStopped":21,"lastUpdateSubmitDate":409,"lastUpdatePostDateStruct":410,"startDateStruct":413,"completionDateStruct":415,"leadSponsor":417,"locationsCount":418},{"fullName":5,"class":6},"CVRx, Inc.","INDUSTRY",{"primaryOutcomes":8,"secondaryOutcomes":21,"otherOutcomes":21},[9,13,17],{"measure":10,"description":11,"timeFrame":12},"Blood Pressure Changes","The results of an office cuff blood pressure measurement to be obtained from a time point prior to implant and as close to the implant procedure as possible (baseline), at 3- and 6- and 12-months post-implant, and then every 6 months up to 3 years from implant.","Pre-implant baseline to 3 years post-implant",{"measure":14,"description":15,"timeFrame":16},"Cardiovascular Medication Changes","Information on currently-utilized doses of cardiovascular medications will be collected at pre-implant baseline, 3- and 6- and 12-months post-implant, and then every 6 months up to 3 years from implant.","Post-implant enrollment to 3 years post-implant",{"measure":18,"description":19,"timeFrame":20},"Number of Health Care Utilizations","Health care utilization information (e.g. heart failure hospitalizations) is collected at 3- and 6- and 12-months post-implant, and then every 6 months up to 3 years from implant.","3 months post-implant to 3 years post-implant",null,{"allocation":21,"interventionModel":21,"interventionModelDescription":21,"primaryPurpose":21,"observationalModel":23,"timePerspective":24,"maskingInfo":21},"COHORT","PROSPECTIVE","Summary:\n\nThe CVRx BAROSTIM THERAPY in Resistant Hypertension Registry will be performed with subjects who have been recently implanted with the BAROSTIM NEO System in accordance with CE-Mark approved criteria for resistant hypertension. Subjects must be enrolled within 30 days from implant. Up to 500 subjects will be enrolled at up to 50 sites. Data should be obtained from standard of care measurements taken prior to implant, at enrollment\u002Fbaseline, and at 3, 6, and 12 months after the device was implanted. After 12 months, data may be obtained in six month intervals for up to three years after implant, at which time each subject will be exited from the registry.\n\nEligibility:\n\nSubjects must sign an Ethics Committee (EC) approved informed consent form for the registry to participate.\n\nSubjects can be included in the Hypertension Registry if they were implanted in the past 30 days and meet the CE-Mark approved indications and contraindications for the BAROSTIM NEO System in the treatment of resistant hypertension. These include:\n\n* Indications\n\n  * Systolic blood pressure greater than or equal to 140 mmHg, and\n  * Resistance to maximally tolerated therapy with a diuretic and two other anti-hypertension medications\n* Contraindications\n\n  * Bilateral carotid bifurcations located above the level of the mandible\n  * Baroreflex failure or autonomic neuropathy\n  * Uncontrolled, symptomatic cardiac bradyarrhythmias\n  * Carotid atherosclerosis that is determined by ultrasound or angiographic evaluation to be greater than 50%\n  * Ulcerative plaques in the carotid artery as determined by ultrasound or angiographic evaluation","Subjects can be included in the Hypertension Registry if they were implanted in the past 30 days and meet the CE-Mark approved indications and contraindications for the BAROSTIM NEO System in the treatment of resistant hypertension.",[28],{"type":29,"name":30,"description":21,"armGroupLabels":21,"otherNames":21},"DEVICE","BAROSTIM NEO™ 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Schwenger",{"facility":356,"status":64,"city":357,"state":21,"zip":358,"country":48,"countryCode":49,"cosmosGeoPoint":359,"geoPoint":363,"contacts":364},"Klinikum Tuttlingen","Tuttlingen","78532",{"type":51,"coordinates":360},[361,362],8.8177,47.98464,{"lat":362,"lon":361},[365,369],{"name":366,"role":39,"phone":367,"phoneExt":21,"email":368},"Ida Weber","+49 7461 97 1415","i.weber@klinikum-tut.de",{"name":370,"role":79,"phone":21,"phoneExt":21,"email":21},"Michael Kotzerke",{"facility":372,"status":45,"city":373,"state":21,"zip":374,"country":48,"countryCode":49,"cosmosGeoPoint":375,"geoPoint":379,"contacts":21},"Heinrich-Braun Klinikum","Zwickau","08060",{"type":51,"coordinates":376},[377,378],12.48839,50.72724,{"lat":378,"lon":377},{"facility":381,"status":45,"city":382,"state":21,"zip":383,"country":384,"countryCode":385,"cosmosGeoPoint":386,"geoPoint":390,"contacts":21},"Maastricht University Medical Center","Maastricht","6229","Netherlands","NL",{"type":51,"coordinates":387},[388,389],5.68889,50.84833,{"lat":389,"lon":388},{"type":392,"investigatorFullName":21,"investigatorTitle":21,"investigatorAffiliation":21,"oldNameTitle":21,"oldOrganization":21},"SPONSOR","100276617","barostim-therapy-in-resistant-hypertension-100276617",false,"NCT02880631","BAROSTIM THERAPY™ In Resistant Hypertension","BAROSTIM THERAPY™ In Resistant Hypertension: A Post-Market Registry With the CE-Marked BAROSTIM NEO™ System","Inclusion Criteria:\n\n* Has signed an EC approved informed consent form\n* Has been implanted with the BAROSTIM NEO system in the past 30 days\n* Systolic blood pressure greater than or equal to 140 mmHg, and\n* Resistance to maximally tolerated therapy with a diuretic and two other anti-hypertension medications\n\nExclusion Criteria:\n\n* Bilateral carotid bifurcations located above the level of the mandible\n* Baroreflex failure or autonomic neuropathy\n* Uncontrolled, symptomatic cardiac bradyarrhythmias\n* Carotid atherosclerosis that is determined by ultrasound or angiographic evaluation to be greater than 50%\n* Ulcerative plaques in the carotid artery as determined by ultrasound or angiographic evaluation","ALL",{"count":402,"type":403},500,"ESTIMATED","3 Years","OBSERVATIONAL","The purpose of this registry (NCT02880631) is to evaluate the effect of BAROSTIM THERAPY with the BAROSTIM NEO System in the commercial setting in subjects recently implanted under the CE-Marked indication for resistant hypertension.",[408],"Hypertension","2026-09-09",{"date":411,"type":412},"2026-09-11","ACTUAL",{"date":414,"type":412},"2016-12-13",{"date":416,"type":403},"2027-07",{"name":5,"class":6},26]