[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100613570":3},{"organization":4,"armGroups":7,"interventions":30,"overallOfficials":36,"centralContacts":49,"locations":55,"responsibleParty":141,"collaborators":36,"id":145,"slug":146,"hasResults":147,"nctId":148,"briefTitle":149,"officialTitle":150,"acronym":36,"eligibilityCriteria":151,"healthyVolunteers":147,"sex":152,"minAge":153,"maxAge":36,"enrollmentInfo":154,"targetDuration":36,"studyType":157,"phases":158,"briefSummary":160,"conditions":161,"keywords":36,"overallStatus":58,"whyStopped":36,"lastUpdateSubmitDate":163,"lastUpdatePostDateStruct":164,"startDateStruct":167,"completionDateStruct":169,"leadSponsor":171,"locationsCount":172},{"fullName":5,"class":6},"Rigshospitalet, Denmark","OTHER",[8,14,20,25],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm 1: Continue Drug D","ACTIVE_COMPARATOR","Participants continue their usual treatment with Drug Dupi throughout the study.",[13],"Drug: DUPIXENT®",{"label":15,"type":16,"description":17,"interventionNames":18},"Arm 2: Stop Drug D","EXPERIMENTAL","Participants discontinue Drug Dupi at baseline and receive no active treatment during the study.",[19],"Other: Dupi discontinuation",{"label":21,"type":10,"description":22,"interventionNames":23},"Arm 3: Continue Drug M","Participants continue their usual treatment with Drug Mepo throughout the study.",[24],"Drug: NUCALA®",{"label":26,"type":16,"description":27,"interventionNames":28},"Arm 4: Stop Drug M","Participants discontinue Drug Mepo at baseline and receive no active treatment during the study.",[29],"Other: Mepo discontinuation",[31,37,41,45],{"type":32,"name":33,"description":34,"armGroupLabels":35,"otherNames":36},"DRUG","DUPIXENT®","Continue Dupixent",[9],null,{"type":32,"name":38,"description":39,"armGroupLabels":40,"otherNames":36},"NUCALA®","\"Continue Nucala",[21],{"type":6,"name":42,"description":43,"armGroupLabels":44,"otherNames":36},"Dupi discontinuation","Stop taking Dupixent at baseline; no substitute is given",[15],{"type":6,"name":46,"description":47,"armGroupLabels":48,"otherNames":36},"Mepo discontinuation","Stop taking Nucala at baseline; no substitute is given",[26],[50],{"name":51,"role":52,"phone":53,"phoneExt":36,"email":54},"Kasper Aanæs, md, phd","CONTACT","60708594","kasperaanaes@hotmail.com",[56,73,87,100,115,130],{"facility":57,"status":58,"city":59,"state":60,"zip":61,"country":62,"countryCode":63,"cosmosGeoPoint":64,"geoPoint":69,"contacts":70},"Rigshospitalet","RECRUITING","Copenhagen","Region H","2100","Denmark","DK",{"type":65,"coordinates":66},"Point",[67,68],12.56553,55.67594,{"lat":68,"lon":67},[71],{"name":72,"role":52,"phone":53,"phoneExt":36,"email":36},"Kasper aanæs, md, phd",{"facility":74,"status":58,"city":75,"state":60,"zip":76,"country":62,"countryCode":63,"cosmosGeoPoint":77,"geoPoint":81,"contacts":82},"Nordsjællands hospital","Hillerød","3400",{"type":65,"coordinates":78},[79,80],12.30081,55.92791,{"lat":80,"lon":79},[83],{"name":84,"role":52,"phone":85,"phoneExt":36,"email":86},"Grethe Samuelsen","48293825","noh.nordsjaellands-hospital@regionh.dk",{"facility":88,"status":58,"city":89,"state":90,"zip":91,"country":62,"countryCode":63,"cosmosGeoPoint":92,"geoPoint":96,"contacts":97},"Køge øre næse hals afd","Køge","Region Sj","4600",{"type":65,"coordinates":93},[94,95],12.18214,55.45802,{"lat":95,"lon":94},[98],{"name":99,"role":52,"phone":36,"phoneExt":36,"email":36},"Bent Ivan Larsen",{"facility":101,"status":58,"city":102,"state":103,"zip":104,"country":62,"countryCode":63,"cosmosGeoPoint":105,"geoPoint":109,"contacts":110},"Dept. of otorhinolaryngology, Odense","Odense","Region Syd","5000",{"type":65,"coordinates":106},[107,108],10.38831,55.39594,{"lat":108,"lon":107},[111],{"name":112,"role":52,"phone":113,"phoneExt":36,"email":114},"Anette Drøhse Kjeldsen","65414314","anette.kjeldsen@rsyd.dk",{"facility":116,"status":58,"city":117,"state":118,"zip":119,"country":62,"countryCode":63,"cosmosGeoPoint":120,"geoPoint":124,"contacts":125},"Vejle sygehus","Vejle","Region S","7100",{"type":65,"coordinates":121},[122,123],9.5357,55.70927,{"lat":123,"lon":122},[126],{"name":127,"role":52,"phone":128,"phoneExt":36,"email":129},"Lars Christian Meyer","79405000","lars.christian.meyer@rsyd.dk",{"facility":131,"status":58,"city":132,"state":36,"zip":36,"country":62,"countryCode":63,"cosmosGeoPoint":133,"geoPoint":137,"contacts":138},"Gødstrup Hospital","Gødstrup",{"type":65,"coordinates":134},[135,136],8.89276,56.15584,{"lat":136,"lon":135},[139],{"name":140,"role":52,"phone":36,"phoneExt":36,"email":36},"Adnan Madzak",{"type":142,"investigatorFullName":143,"investigatorTitle":144,"investigatorAffiliation":5,"oldNameTitle":36,"oldOrganization":36},"PRINCIPAL_INVESTIGATOR","Kasper Aanaes","Medical doctor, phd., Principal investigator, associated professor","100613570","phase-4-complete-remission-after-treatment-with-biologics-for-nasal-polyps-100613570",false,"NCT07268313","Complete Remission After Treatment With Biologics for Nasal Polyps","English Title: Complete Remission Study Subtitle: Discontinuation of Mepolizumab or Dupilumab After at Least 12 Months Without Symptoms in Patients With Severe Chronic Rhinosinusitis With Polyps - a National Danish RCT Study","Inclusion Criteria:\n\n5.1 Inclusion criteria (all must be fulfilled)\n\nInclusion criteria:\n\nAt the time when the patient started biological treatment, they must have fulfilled the EPOS criteria for initiation of biologic treatment (REF EPOS):\n\n* Fulfil the criteria for CRSwNP\n* Presence of bilateral polyps in a patient\n* Had ESS (sinus surgery) (exceptional circumstances excluded)\n* Fulfil at least three of the following five criteria Evidence of type 2 inflammation Need for (and treated with) systemic corticosteroids or contraindication to these SNOT-22 score of 40 or above Significant loss of smell Asthma needing regular inhaled corticosteroids\n\nTo enter this study, the patient must be:\n\n* Above 18 years of age\n* Currently be in treatment with either Dupilumab (300 mg) or Mepolizumab (100 mg) with treatment every fourth week. This treatment should have been stable\u002Funchanged for at least three months.\n* Within the latest year, the patient must at all times have scored all the below symptoms of CRS five or below on a VAS scale from 0 - 10 - Doing this, it is according to the EPOS defined as controlled disease. The items are: nasal blockage, rhinorrhea\u002Fpostnasal drip, facial pain\u002Fpressure, smell, sleep disturbance or fatigue) Please view appendix 2.\n* Within the latest year the nasal endoscopy cannot have showed polyp score of more than 1+1 out of 4+4, further, no thick secretions or general oedema must have been present.\n* Within the latest year the patient is not allowed to have had ESS or rescue treatment for their CRSwNP (antibiotics or systemic steroids)\n* The patient must be able to understand Danish and able to sign an informed content.\n\nExclusion Criteria:\n\n* In the twelve months of remission the patient is not allowed to have had AECRS (acute exacerbation of chronic rhinosinusitis). A common cold is allowed.\n* Polyp removal in the out-patient clinic may not have been performed within the last 3 months.\n* In the twelve months of remission the patient cannot at any time have scored higher than 1.2 on the ACQ questionnaire, meaning that the patient does not have uncontrolled asthma (Appendix 3).\n* Patients who, because of language barriers, are not able to understand written information and, thus, are not able to answer questionnaires.\n* Patients who currently receive biologics for any other disease (asthma not included)\n* Patients who are not able to give informed consent (i.e., patients who are permanently incapable)\n* Patients who are not eligible because of the investigator's judgement\n* Patients who experience pregnancy during the study will be excluded after an unscheduled visit (LOCF) - active IVF treatment. (Please look belove)\n* Patients who have or recently have had illness, such as cancer that or its treatment is expected to significantly affect morbidity and\u002For quality of life in the next two years\n* Unwillingness to follow the study procedure\n* Hypersensitivity to any of either Dupilumab or Mepolizumab.","ALL","18 Years",{"count":155,"type":156},66,"ESTIMATED","INTERVENTIONAL",[159],"PHASE4","In this RCT the investigators randomize patients who are treated with biologic treatment (Nucala or Dupixent) due to nasal polyps and have controlled disease within the last year to either stop treatment og continue as a control group.",[162],"Nasal Polyps","2025-11-25",{"date":165,"type":166},"2025-12-05","ACTUAL",{"date":168,"type":166},"2025-04-03",{"date":170,"type":156},"2027-06-01",{"name":5,"class":6},6]