[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of Fribourg\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":77},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100601662","influence-of-tea-extract-on-maximal-voluntary-knee-contraction-following-downhill-jogging-100601662",false,"NCT07113405","Influence of Tea Extract on Maximal Voluntary Knee Contraction Following Downhill Jogging","The Influence of Tea Extract on Maximal Voluntary Knee Contraction After 30 Minutes of Downhill Jogging: a Randomized, Double-blind, Placebo-controlled Study","ITMVC-DJ","Inclusion Criteria:\n\n* Signed written informed consent\n* Aged between 18-40 years\n* Healthy subjects\n\nExclusion Criteria:\n\n* Any type of food allergy (e.g. nuts)\n* Health-related problems according to the \"Physical Activity Readiness Questionnaire (PAR-Q)\n* Current injury of the lower extremities\n* Serious clinical back pain or current back injuries\n* Orthopedic disorders\n* Cardiovascular diseases\n* Current Intake of blood-thinning medication\n* Current Intake of anti-inflammatory medication",true,"ALL","18 Years","40 Years",{"count":22,"type":23},60,"ESTIMATED","INTERVENTIONAL",[26],"NA","In this research project, we want to investigate whether the combined intake of proteins and tea extract has an influence on muscle regeneration compared to the sole intake of proteins or a placebo product. In the study, you will be randomly assigned to one of 3 groups. Neither the research group nor you will know which group you are assigned to. The study lasts 5 days for you as a participant. During these 5 days you will have to attend a total of 5 appointments in our laboratory. The groups differ only in the intake of the regeneration product, otherwise all measurements and appointments are identical. You will jog downhill for 30 minutes on the first day in order to strain your muscles. In order to be able to draw conclusions about the regeneration of your muscles, we will carry out the following measurements on all 5 days: Blood sampling at the fingertip, ultrasound of the thigh muscle, pain tolerance of the thigh muscle, strength tests of the thigh muscle, muscle function of the thigh muscle and jumping performance.",[29],"Muscle Recovery",[31,32,33,34],"Protein","muscle recovery","Tea extract","EIMD","RECRUITING","2026-05-01",{"date":38,"type":39},"2026-05-04","ACTUAL",{"date":41,"type":39},"2025-12-01",{"date":43,"type":23},"2026-12-30",{"name":45,"class":46},"University of Fribourg","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":56,"minAge":19,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":24,"phases":59,"briefSummary":60,"conditions":61,"keywords":66,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":47},"100589790","confocal-histolog-scanner-in-routine-breast-conserving-surgery-chib-100589790","NCT06958991","Confocal Histolog Scanner in Routine Breast-Conserving Surgery (CHiB)","Confocal Histolog Scanner in Routine Breast-Conserving Surgery","CHiB","Inclusion Criteria:\n\n* Adult female Subject ≥18 years old.\n* Subject scheduled for breast conserving surgery of invasive and\u002For in-situ ductal and lobular carcinoma.\n* Subject is able to read, understand and sign the informed consent.\n\nExclusion Criteria:\n\n* Subject with planned mastectomy\n* Subject does not speak French- Subject with planned tumor-adapted breast reduction\n* Subject is pregnant\u002F lactating. Subjects pregnant\u002Flactating are excluded because such subjects are presenting additional risks during the surgery and they are also rare.\n* Participation in any other clinical study that would affect data acquisition.","FEMALE",{"count":58,"type":23},100,[26],"The clinical performance study is collecting data from the use of a CE mark product used within the scope of its intended purpose to intraoperatively visualize tissue specimen. The subjects are not submitted to invasive and burdensome procedures compared to the standard of care surgical practices and regular use of the CE mark product.",[62,63,64,65],"Breast Cancer Invasive","Breast Cancer Surgery","Lumpectomy","Confocal Laser Endomicroscopy",[67,68],"breast cancer surgery","confocal microscopy","2025-11-22",{"date":71,"type":39},"2025-11-25",{"date":73,"type":39},"2025-06-01",{"date":75,"type":23},"2026-09-30",{"name":45,"class":46},""]