[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100054231":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":39,"centralContacts":47,"locations":56,"responsibleParty":91,"collaborators":94,"id":96,"slug":97,"hasResults":98,"nctId":99,"briefTitle":100,"officialTitle":100,"acronym":101,"eligibilityCriteria":102,"healthyVolunteers":98,"sex":103,"minAge":104,"maxAge":28,"enrollmentInfo":105,"targetDuration":28,"studyType":108,"phases":109,"briefSummary":111,"conditions":112,"keywords":114,"overallStatus":120,"whyStopped":28,"lastUpdateSubmitDate":121,"lastUpdatePostDateStruct":122,"startDateStruct":125,"completionDateStruct":127,"leadSponsor":129,"locationsCount":130},{"fullName":5,"class":6},"Ottawa Hospital Research Institute","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Spironolactone","EXPERIMENTAL","Spironolactone 25 mg daily",[13],"Drug: Spironolactone (drug)",{"label":15,"type":16,"description":17,"interventionNames":18},"Standard first-line antihypertensive therapy","ACTIVE_COMPARATOR","Participants randomized to standard therapy will undergo secondary randomization to candesartan (8 mg daily), hydrochlorothiazide (25 mg daily), or amlodipine (5 mg daily)",[19,20,21],"Drug: Candesartan 8mg","Drug: Hydrochlorothiazide (HCTZ) 25 milligrams.","Drug: Amlodipine (5mg)",[23,29,33,36],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":28},"DRUG","Spironolactone (drug)","Spironolactone 25 mg daily: Spironolactone is a widely available and inexpensive MR antagonist medication which blocks the action of aldosterone. Spironolactone is the most commonly recommended drug for the treatment of primary aldosteronism given its efficacy in improving blood pressure and reducing cardiovascular and kidney disease risk for this patient population, with 25 mg being the standard starting dose.",[9],null,{"type":24,"name":30,"description":31,"armGroupLabels":32,"otherNames":28},"Candesartan 8mg","Comparator medications were selected because they represent common guideline-recommended first-line antihypertensive therapies from mechanistically distinct drug classes routinely used in contemporary primary care practice and hypertension guidelines. Doses were selected based on equivalent defined daily doses (DDD). The purpose of including multiple comparator therapies is to emulate real-world first-line prescribing practices in primary care rather than compare spironolactone against a single mechanistic alternative.",[15],{"type":24,"name":34,"description":31,"armGroupLabels":35,"otherNames":28},"Hydrochlorothiazide (HCTZ) 25 milligrams.",[15],{"type":24,"name":37,"description":31,"armGroupLabels":38,"otherNames":28},"Amlodipine (5mg)",[15],[40,44],{"name":41,"affiliation":42,"role":43},"Sharon Johnston, MD","Institut du Savoir Montfort","PRINCIPAL_INVESTIGATOR",{"name":45,"affiliation":46,"role":43},"Gregory L Hundemer, MD","The Ottawa Hospital",[48,53],{"name":45,"role":49,"phone":50,"phoneExt":51,"email":52},"CONTACT","(613) 738-8400","81885","ghundemer@toh.ca",{"name":54,"role":49,"phone":28,"phoneExt":28,"email":55},"Deena Fremont, MSc","dfremont@ohri.ca",[57,71,82],{"facility":46,"status":28,"city":58,"state":59,"zip":60,"country":61,"countryCode":62,"cosmosGeoPoint":63,"geoPoint":68,"contacts":69},"Ottawa","Ontario","K1H 7W9","Canada","CA",{"type":64,"coordinates":65},"Point",[66,67],-75.69812,45.41117,{"lat":67,"lon":66},[70],{"name":45,"role":49,"phone":50,"phoneExt":51,"email":52},{"facility":72,"status":28,"city":58,"state":59,"zip":73,"country":61,"countryCode":62,"cosmosGeoPoint":74,"geoPoint":76,"contacts":77},"Ottawa Nurse Practitioner-Led Clinic","K1L 8L8",{"type":64,"coordinates":75},[66,67],{"lat":67,"lon":66},[78],{"name":79,"role":49,"phone":80,"phoneExt":28,"email":81},"Hoda Mankal, NP","(613) 366-4742","hmankal@ottawanplc.org",{"facility":83,"status":28,"city":84,"state":59,"zip":85,"country":61,"countryCode":62,"cosmosGeoPoint":28,"geoPoint":28,"contacts":86},"St-Isidore Médical","Saint Isidore","K0C 2B0",[87],{"name":88,"role":49,"phone":89,"phoneExt":28,"email":90},"Manon Denis-LeBlanc, MD","(613) 524-3225","manondenisleblanc@montfort.on.ca",{"type":43,"investigatorFullName":92,"investigatorTitle":93,"investigatorAffiliation":5,"oldNameTitle":28,"oldOrganization":28},"Greg Hundemer","Clinician Scientist",[95],{"name":46,"class":6},"100054231","phase-4-spiro-first-a-pragmatic-primary-care-embedded-pilot-trial-of-renin-guided-first-line-antihypertensive-therapy-100054231",false,"NCT07687160","SPIRO-First: A Pragmatic Primary Care-Embedded Pilot Trial of Renin-Guided First-Line Antihypertensive Therapy","SPIRO-First","Inclusion Criteria:\n\n1. Age ≥18 years.\n2. Under the care of a primary care clinician in Ontario.\n3. Standardized office systolic blood pressure ≥130 mmHg or diastolic blood pressure ≥80 mmHg.\n4. Mean daytime baseline ABPM systolic blood pressure ≥130 mmHg or diastolic blood pressure ≥80 mmHg.\n5. Treating primary care clinician has independently determined that initiation of antihypertensive pharmacotherapy is clinically indicated.\n6. Either:\n\n   * Not currently receiving antihypertensive therapy, OR\n   * Receiving a single antihypertensive medication (ACE inhibitor, ARB, thiazide\u002Fthiazide-like diuretic, or calcium channel blocker) which the treating primary care clinician considers safe to discontinue for a 2-week washout period.\n7. Suppressed renin defined as direct renin concentration \\\u003C6 ng\u002FL (\\\u003C10 mU\u002FL) measured under routine outpatient conditions. Suppressed renin was selected as the primary biologic enrichment criterion because it is the physiologic hallmark of sodium-retaining, aldosterone-mediated hypertension and is more pragmatically scalable in primary care than complex biochemical primary aldosteronism (PA) definitions.\n8. In the opinion of the treating primary care clinician, outpatient participation in the study is appropriate.\n\nExclusion Criteria:\n\n1. Standardized office systolic blood pressure \\>170 mmHg if untreated OR \\>150 mmHg if receiving one antihypertensive medication.\n2. Known diagnosis of PA requiring specialist-directed management.\n3. Known secondary hypertension requiring disease-specific therapy.\n4. Current use of MR antagonists.\n5. Known intolerance or contraindication to spironolactone, candesartan, hydrochlorothiazide, or amlodipine.\n6. eGFR \\\u003C30 mL\u002Fmin\u002F1.73 m2.\n7. Serum potassium ≥5.0 mmol\u002FL.\n8. Serum sodium \\\u003C135 mmol\u002FL.\n9. Pregnancy, breastfeeding, or intention to become pregnant during the study period. Women of childbearing potential must have a negative pregnancy test prior to randomization.\n10. Participation in another interventional study likely to affect blood pressure.\n11. Inability to provide consent","ALL","18 Years",{"count":106,"type":107},30,"ESTIMATED","INTERVENTIONAL",[110],"PHASE4","The goal of this clinical trial is to determine whether a renin-guided antihypertensive treatment strategy is feasible to implement in community primary care clinics and to explore whether spironolactone improves blood pressure control in adults with low-renin hypertension.\n\nThe main questions it aims to answer are:\n\nIs it feasible to identify, recruit, randomize, and follow adults with low-renin hypertension in a pragmatic primary care-based clinical trial?\n\nDoes first-line treatment with spironolactone result in greater reductions in ambulatory blood pressure compared with standard first-line antihypertensive therapy among adults with low-renin hypertension?\n\nResearchers will compare spironolactone 25 mg daily with standard first-line antihypertensive therapy (candesartan, hydrochlorothiazide, or amlodipine) to determine whether spironolactone provides better blood pressure control in adults with low-renin hypertension.\n\nParticipants will:\n\nUndergo blood pressure assessments, blood tests, and ambulatory blood pressure monitoring (ABPM) to determine eligibility.\n\nBe randomly assigned to receive either spironolactone or a standard first-line antihypertensive medication for 12 weeks.\n\nComplete follow-up visits and laboratory testing to monitor blood pressure response, kidney function, electrolyte levels, medication adherence, and side effects.\n\nUndergo repeat blood pressure measurements and ABPM at the end of the study.",[113],"Hypertension",[115,116,117,9,118,119],"hypertension","Renin-Guided Therapy","Antihypertensive treatment","Precision Medicine","Primary aldosteronism","NOT_YET_RECRUITING","2026-07-10",{"date":123,"type":124},"2026-07-13","ACTUAL",{"date":126,"type":107},"2026-09-01",{"date":128,"type":107},"2028-02",{"name":5,"class":6},3]