[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100562338":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":12,"centralContacts":12,"locations":12,"responsibleParty":25,"collaborators":29,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":38,"acronym":39,"eligibilityCriteria":40,"healthyVolunteers":41,"sex":42,"minAge":43,"maxAge":44,"enrollmentInfo":45,"targetDuration":12,"studyType":48,"phases":49,"briefSummary":51,"conditions":52,"keywords":12,"overallStatus":57,"whyStopped":12,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":12},{"fullName":5,"class":6},"Universitair Ziekenhuis Brussel","OTHER",[8,13],{"label":9,"type":10,"description":11,"interventionNames":12},"100 patients without R-Support supplementation (control group)","NO_INTERVENTION","These patients will have no intervention, will not take the nutritional supplements",null,{"label":14,"type":15,"description":16,"interventionNames":17},"100 patients with R-Support supplementation (intervention group)","ACTIVE_COMPARATOR","The treatment period for the intervention group will last 28 days, divided into two phases: 14 days preoperative and 14 days postoperative.\n\nDuring the preoperative phase, participants will consume one shake per day. Each shake will consist of 35 grams (3 scoops) of R-Support Prepare mixed with 250 milliliters of water or milk. This regimen will be followed for 14 days leading up to the surgery.\n\nDuring the postoperative phase, participants will consume one shake per day. Each shake will consist of 35 grams (3 scoops) of R-Support After mixed with 250 milliliters of water or milk. This regimen will be followed for 14 days following the surgery.",[18],"Dietary Supplement: R-Support Prepare & After nutritional supplement",[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":12},"DIETARY_SUPPLEMENT","R-Support Prepare & After nutritional supplement","R-Support is a nutritional supplement containing proteins, Vitamine A, Vitamine B6, Vitamine B11, Vitamine B12, Vitamine C, Vitamine D3, Vitamine E, IJzer, Koper, Selenium, Zink, Magnesium, Omega-3 and Beta-glucanen.",[14],{"type":26,"investigatorFullName":27,"investigatorTitle":28,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"PRINCIPAL_INVESTIGATOR","Letizia Georgiou","Research Fellow in Plastic Surgery",[30,32],{"name":31,"class":6},"Chirec",{"name":33,"class":6},"Zuyderland Medical Centre","100562338","phase-4-the-impact-of-nutritional-optimization-to-enhance-postoperative-outcomes-using-the-r-support-supplements-100562338",false,"NCT06601868","The Impact of Nutritional Optimization to Enhance Postoperative Outcomes Using the R-Support Supplements","R-Support","Inclusion Criteria:\n\n* ASAI\\&II\n* Age 18-65\n* Type of surgery:\n\n  * Abdominoplasty o Breast reduction\n  * Breast reconstruction through a DIEaP-flap\n  * Extensive circumferential liposuction and body contouring surgery\n\nExclusion Criteria:\n\n* Patients with systemic illness, including:\n\n  * Diabetes\n  * Immune deficiencies\n  * Severe cardiovascular disease\n  * Renal insufficiency\n* Active smokers or smokers that didn't quit 4 weeks prior to surgery\n* Patients under chemotherapy (Patients currently undergoing chemotherapy are not allowed to participate in this study. Patient undergoing previous chemotherapy are allowed to participate in this study, as long as the chemotherapy ended 6 months before the planned surgery and are currently in remission or free of disease.)\n* Patients after bariatric surgery with partial or complete stomachresection\n* Patients taking SSRI medication\n* Pregnancy\n* ASAIII\\&IV\n* Gluten intolerance\n* Lactose intolerance\n* Allergy or hypersensitivity to fish, soya, milk, shellfish.",true,"ALL","18 Years","65 Years",{"count":46,"type":47},200,"ESTIMATED","INTERVENTIONAL",[50],"PHASE4","The aim of this pilot study is to evaluate the potential benefits of nutrient supplementation on post-operative recovery for patients undergoing certain types of surgery, compared to those who do not receive such supplementation. The multi-center study will be conducted in Belgium and the Netherlands at UZ Brussel, Delta CHIREC, and Zuyderland Medical Center.\n\nThe pilot study will serve as a precursor to a randomized controlled trial and will include 200 patients. Participants must be classified as ASA I or II, aged between 18 and 65, and undergoing abdominoplasty, breast reduction, breast reconstruction through a DIEP-flap, or extensive circumferential liposuction and body contouring surgery.\n\nEligible patients who provide informed consent will be randomly assigned to either the intervention group, receiving R-Support supplementation, or the control group, without supplementation. Each group will consist of 100 patients. The study will span 8 weeks, with a 2-week preoperative period and a 6-week postoperative period. The treatment will involve a 28-day supplementation period, with R-Support Recover Prepare given 14 days preoperatively and R-Support Recover After given 14 days postoperatively.\n\nPostoperative recovery will be assessed using the PRP-Questionnaire and Functional Recovery Index, which together will measure physical and psychological recovery, as well as the speed of recovery in the early postoperative phase. The study hypothesizes that the intervention group will experience quicker recovery than the control group. Additionally, data on hospital stay duration and early postoperative complications will be collected, with the expectation that better-prepared bodies will recover faster, potentially leading to fewer hospitalized days and complications. The study aims to demonstrate enhanced postoperative recovery, reduced early complications (such as wound dehiscence and infection), and shorter hospital stays.",[53,54,55,56],"Abdominoplasty","Breast Reduction","Autologous Breast Reconstruction","Body Contouring Surgery","NOT_YET_RECRUITING","2024-09-18",{"date":60,"type":61},"2024-09-20","ACTUAL",{"date":63,"type":47},"2024-10-01",{"date":65,"type":47},"2025-12-31",{"name":5,"class":6}]