[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100623482":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":14,"centralContacts":20,"locations":25,"responsibleParty":39,"collaborators":10,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":10,"eligibilityCriteria":46,"healthyVolunteers":47,"sex":48,"minAge":49,"maxAge":10,"enrollmentInfo":50,"targetDuration":10,"studyType":53,"phases":10,"briefSummary":54,"conditions":55,"keywords":10,"overallStatus":58,"whyStopped":10,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":63,"completionDateStruct":64,"leadSponsor":66,"locationsCount":67},{"fullName":5,"class":6},"Medical University of Gdansk","OTHER",[8,11],{"label":9,"type":10,"description":9,"interventionNames":10},"Healthy Volunteers",null,{"label":12,"type":10,"description":13,"interventionNames":10},"Critically ill","Patients Hospitalized in the ICU",[15,18],{"name":16,"affiliation":5,"role":17},"Karol P. Steckiewicz, MD, PhD","PRINCIPAL_INVESTIGATOR",{"name":19,"affiliation":5,"role":17},"Radosław Owczuk, MD, PhD, DSc, Prof.",[21],{"name":16,"role":22,"phone":23,"phoneExt":10,"email":24},"CONTACT","+48 58 349 32 80","karol.steckiewicz@gumed.edu.pl",[26],{"facility":27,"status":10,"city":28,"state":10,"zip":10,"country":29,"countryCode":30,"cosmosGeoPoint":31,"geoPoint":36,"contacts":37},"Medical University of Gdanks","Gdansk","Poland","PL",{"type":32,"coordinates":33},"Point",[34,35],18.64912,54.35227,{"lat":35,"lon":34},[38],{"name":16,"role":22,"phone":23,"phoneExt":10,"email":24},{"type":40,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100623482","assessment-of-the-repeatability-of-sublingual-microcirculation-function-measurements-in-healthy-volunteers-and-critically-ill-patients-100623482",false,"NCT07397208","Assessment of the Repeatability of Sublingual Microcirculation Function Measurements in Healthy Volunteers and Critically Ill Patients","Group 1: Healthy Volunteers\n\nInclusion Criteria:\n\n* ASA Physical Status I-II\n* Age 18-40 years\n\nExclusion Criteria:\n\n* Chronic diseases\n* Chronic medication use\n* Pregnancy\n* Use of stimulants (caffeine, nicotine, alcohol) within 12 hours prior to the study\n* Lack of consent to participate\n\nGroup 2: Patients Hospitalized in the ICU\n\nInclusion Criteria:\n\n* Age \\> 18 years\n* Hospitalization in the Intensive Care Unit (ICU)\n* Requirement for vasoactive drugs (minimum norepinephrine equivalent dose \\>0.1μg\u002Fkg \u002F min )\n* Mechanical ventilation via an endotracheal tube\n\nExclusion Criteria:\n\n* Head and craniofacial trauma\n* Pregnancy\n* Intensive fluid therapy (\\>200ml\u002Fh)\n* Changes in vasoactive drug dosages within 30 minutes prior to study inclusion\n* Hypothermia (body temperature \\\u003C35.5 oC)\n* Fever (body temperature \\>38.5oC)",true,"ALL","18 Years",{"count":51,"type":52},200,"ESTIMATED","OBSERVATIONAL","The assessment of microcirculatory function plays a pivotal role in perioperative medicine and intensive care. One promising method for evaluating microcirculatory function is the microscopic analysis of the oral mucosal microvasculature. However, this method is not currently fully validated.\n\nThe aim of this study is to assess the repeatability of sublingual microcirculation measurements using the CytoCam-IDF device (Braedius Medical).",[56,57],"Critical Illness","Healthy","NOT_YET_RECRUITING","2026-02-07",{"date":61,"type":62},"2026-02-10","ACTUAL",{"date":59,"type":52},{"date":65,"type":52},"2029-02-01",{"name":5,"class":6},1]