[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100454119":3},{"organization":4,"armGroups":7,"interventions":28,"overallOfficials":37,"centralContacts":41,"locations":46,"responsibleParty":93,"collaborators":97,"id":102,"slug":103,"hasResults":104,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":108,"eligibilityCriteria":109,"healthyVolunteers":104,"sex":110,"minAge":111,"maxAge":24,"enrollmentInfo":112,"targetDuration":24,"studyType":115,"phases":116,"briefSummary":118,"conditions":119,"keywords":123,"overallStatus":49,"whyStopped":24,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":134},{"fullName":5,"class":6},"Odense University Hospital","OTHER",[8,14,20,25],{"label":9,"type":10,"description":11,"interventionNames":12},"RCT group - Placebo","PLACEBO_COMPARATOR","Included patients with an AddiQoL-30 score \\\u003C 85 and\u002For short Synacthen test stimulated plasma cortisol levels \\> 100 and \\\u003C 420 nmol\u002FL that are radomized to recieve placebo tablets.",[13],"Drug: Placebo",{"label":15,"type":16,"description":17,"interventionNames":18},"RCT group - Hydrocortisone","ACTIVE_COMPARATOR","Included patients with an AddiQoL-30 score \\\u003C 85 and\u002For short Synacthen test stimulated plasma cortisol levels \\> 100 and \\\u003C 420 nmol\u002FL that are radomized to recieve hydrocortisone tablets.",[19],"Drug: Hydrocortisone",{"label":21,"type":22,"description":23,"interventionNames":24},"Comparator group 1","NO_INTERVENTION","Patients with an AddiQoL-30 score \\> 85 and short Synacthen test stimulated plasma cortisol level \\> 420 nmol\u002FL. Patients undergo baseline examination only.",null,{"label":26,"type":22,"description":27,"interventionNames":24},"Comparator group 2","Patients with pronounced adrenal insufficiency (short Synacthen test stimulated plasma cortisol levels \\\u003C 100 nmol\u002FL) - regardless of AddiQoL-30 score. These patients undergo baseline examination and commence open hydrocortisone replacement according to standard clinical practice.",[29,34],{"type":30,"name":31,"description":32,"armGroupLabels":33,"otherNames":24},"DRUG","Hydrocortisone","Patients are randomized to oral hydrocortisone (10 mg twice daily) or placebo for 16 weeks.",[15],{"type":30,"name":35,"description":32,"armGroupLabels":36,"otherNames":24},"Placebo",[9],[38],{"name":39,"affiliation":5,"role":40},"Marianne S Andersen","PRINCIPAL_INVESTIGATOR",[42],{"name":39,"role":43,"phone":44,"phoneExt":24,"email":45},"CONTACT","+4565411807","marianne.andersen1@rsyd.dk",[47,64,77],{"facility":48,"status":49,"city":50,"state":24,"zip":24,"country":51,"countryCode":52,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"Department of Endocrinology and Internal Medicine, Aarhus University Hospital","RECRUITING","Aarhus","Denmark","DK",{"type":54,"coordinates":55},"Point",[56,57],10.21076,56.15674,{"lat":57,"lon":56},[60],{"name":61,"role":43,"phone":62,"phoneExt":24,"email":63},"Jens Otto L Jørgensen, Professor","+45 20727383","joj@clin.au.dk",{"facility":65,"status":49,"city":66,"state":24,"zip":24,"country":51,"countryCode":52,"cosmosGeoPoint":67,"geoPoint":71,"contacts":72},"Department of Nephrology and Endocrinology, Rigshospitalet","Copenhagen",{"type":54,"coordinates":68},[69,70],12.56553,55.67594,{"lat":70,"lon":69},[73],{"name":74,"role":43,"phone":75,"phoneExt":24,"email":76},"Ulla Feldt-Rasmussen, Professor","+45 35451023","Ulla.Feldt-Rasmussen@regionh.dk",{"facility":78,"status":49,"city":79,"state":24,"zip":80,"country":51,"countryCode":52,"cosmosGeoPoint":81,"geoPoint":85,"contacts":86},"Department of Endocrinology, Odense University Hospital","Odense","5230",{"type":54,"coordinates":82},[83,84],10.38831,55.39594,{"lat":84,"lon":83},[87,91],{"name":88,"role":43,"phone":89,"phoneExt":24,"email":90},"Marianne S Andersen, Professor","+45 65411807","Marianne.Andersen1@rsyd.dk",{"name":92,"role":40,"phone":24,"phoneExt":24,"email":24},"Marianne Andersen, DMSci",{"type":94,"investigatorFullName":95,"investigatorTitle":96,"investigatorAffiliation":5,"oldNameTitle":24,"oldOrganization":24},"SPONSOR_INVESTIGATOR","Marianne Andersen","Professor",[98,100],{"name":99,"class":6},"Aarhus University Hospital",{"name":101,"class":6},"Copenhagen University Hospital, Denmark","100454119","phase-4-hydrocortisone-and-placebo-in-patients-with-symptoms-of-adrenal-insufficiency-after-cessation-of-glucocorticoid-treatment-100454119",false,"NCT05193396","Hydrocortisone and Placebo in Patients With Symptoms of Adrenal Insufficiency After Cessation of Glucocorticoid Treatment","A Multi-centre, Randomised, Double-blinded, Placebo Controlled 16-weeks Study to Compare the Effect of Hydrocortisone and Placebo in Patients With Giant Cell Arteritis (GCA)\u002F Polymyalgia Rheumatica (PMR) With Patient-reported Symptoms of Adrenal Insufficiency After Cessation of Glucocorticoid Treatment.","REPLACE","Inclusion Criteria:\n\n* Age ≥ 50 years\n* A diagnosis of PMR or GCA in GC free remission for \\>2 week and \\\u003C12 weeks after treatment with prednisolone (any dosage) for ≥12 weeks\n\nExclusion Criteria:\n\n* Known primary or secondary adrenal insufficiency\n* Known Cushing´s syndrome\n* Heart failure (New York Heart Association class IV)\n* Kidney failure with an estimated glomerular filtration rate \\\u003C30 mL\u002Fmin\n* Liver cirrhosis\n* Active cancer\n* Known severe immune deficiency\n* A history of psychiatric disease requiring treatment by a psychiatric department (for affective disorders only if within the last year before study entry)\n* Alcohol consumption \\>21 units per week\n* Planned major surgery during the study period at study entry\n* Use of drugs that interfere with cortisol metabolism\u002Fmeasurements:\n* Systemic oestrogen treatment within 1 month before study inclusion\n* Strong CYP3A4 inhibitors or inducers\n* Use of other glucocorticoid formulations: inhaled, intra-articular or intramuscular injections, creams European steroid group IV applied in genital area\n* Permitted glucocorticoid formulations: eye-drops, nasal spray, creams European group I-III, and European group IV applied in non-genital area\n* Inability to provide written informed consent","ALL","50 Years",{"count":113,"type":114},100,"ESTIMATED","INTERVENTIONAL",[117],"PHASE4","Cortisol, a glucocorticoid (GC) hormone secreted from the adrenal glands, is essential for survival. Cortisol also possesses anti-inflammatory actions and GC formulations (prednisolone) are used to treat many inflammatory diseases and conditions. Indeed, three percent of the Danish population (≈ 180.000 individuals) redeems at least one prescription of synthetic GC per year and at least 20,000 patients annually discontinue GC treatment. Pharmacological GC therapy suppresses endogenous cortisol production and thereby induce relative adrenal insufficiency (GIA). The risk of GIA as determined by the adrenal corticotrophic hormone (ACTH) stimulation test has previously been reported to ≈ 25 %, but testing after GC treatment is not routinely performed. Indeed, new evidence suggest that the risk of GIA after planned cessation of prednisolone treatment for polymyalgia rheumatic (PMR) or giant cell arteritis (GCA) is substantially lower, probably 2%. The reason for this discrepancy is undoubtedly selection bias in the previous publications and the use of inaccurate cortisol assays. At the same time, however, it was observed that 25% exhibited pronounced symptoms of adrenal insufficiency based on a questionnaire specific for detecting symptoms of adrenal insufficiency, the so-called AddiQoL-30. Concomitantly, the basal cortisol levels in the same group were significantly lower as compared to the group, who exhibited milder or no symptoms attributable to adrenal insufficiency. This observation aligns with the clinical experience that PMR\u002FGCA patients often complain of fatigue after planned cessation of prednisolone treatment. This often occurs in the absence of objective symptoms or signs of residual PMR\u002FGCA disease activity. The scenario has been designated as \"the steroid withdrawal syndrome\". This may represent a state of relative adrenal insufficiency prompted by long term, high dose prednisolone treatment. The proper way to tackle this clinical conundrum is to perform a proper randomized trial, which so far has not been conducted.\n\nTherefore, investigators of this study will perform the first placebo-controlled randomised controlled trial (RCT) in patients with PMR and GCA after planned cessation of GC treatment. Investigators argue that neither watchful waiting nor routine hydrocortisone replacement are infallible. The study will be the first evidence-based guidance and aid to GIA patients and thus meet an important need for many thousand patients.",[120,121,122],"Adrenal Insufficiency","Polymyalgia Rheumatica (PMR)","Giant Cell Arteritis (GCA)",[124],"tertiary adrenal insufficiency","2025-12-15",{"date":127,"type":128},"2025-12-22","ACTUAL",{"date":130,"type":128},"2022-02-01",{"date":132,"type":114},"2026-01",{"name":95,"class":6},3]