[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"postoperative-outcomes\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:postoperative-outcomes":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,53,83],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100640235","evaluating-the-feasibility-of-prehabilitation-delivery-models-for-patients-preparing-for-ovarian-cancer-surgery-100640235",false,"NCT07609082","Evaluating the Feasibility of Prehabilitation Delivery Models for Patients Preparing for Ovarian Cancer Surgery","Assessing Delivery Approaches for Prehabilitation Trials in Ovarian Cancer: A Pilot Feasibility Patient-Preference Trial","ADAPT-OC","Inclusion Criteria:\n\n* Female\n* Aged ≥18 years\n* Scheduled for cytoreductive surgery for an ovarian mass suspected or confirmed of cancer\n* Surgery planned ≥3 weeks from time of booking\n* No contraindications to exercise on the CSEP Get Active Questionnaire\n* Able to provide written informed consent\n* Able to understand and communicate in English\n\nExclusion Criteria:\n\n* Pregnancy\n* Surgery scheduled \\\u003C3 weeks from booking\n* Receiving neoadjuvant chemotherapy\n* Positive contraindications to exercise on the CSEP Get Active Questionnaire\n* End-stage or advanced renal disease limiting safe protein supplementation\n* Malnutrition as assessed by a registered dietician","FEMALE","18 Years",{"count":20,"type":21},36,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this clinical trial is to learn whether high-dose multimodal prehabilitation, delivered either in person or remotely with coaching and web application support, is feasible and acceptable for women preparing for ovarian cancer surgery. It will also examine which delivery model patients prefer and the factors influencing patient preferences.\n\nThe main questions ADAPT-OC aims to answer are:\n\n1. Can participants achieve the prescribed aerobic exercise target of at least 10 MET-hours per week before surgery?\n2. Do patients prefer in-person prehabilitation, remote prehabilitation, or education-only care, and what factors influence that preference?\n\nThe researchers will compare in-person prehabilitation, remote prehabilitation, and education-only care to see which delivery approach is most feasible, acceptable, and practical for patients with suspected ovarian cancer.\n\nParticipants will:\n\n* Choose their preferred study group, or be randomly assigned if they have no preference\n* Complete physical assessments, questionnaires, and interviews at baseline, 1-3 days before surgery, and 4 weeks after surgery\n* If assigned to a prehabilitation group, complete aerobic exercise, protein supplementation, and daily breathing exercises before surgery\n* Attend weekly coaching sessions with a trained prehabilitation coach\n* Use the KingstonPrehab web application to track exercise, nutrition, breathing practice, and progress toward activity goals",[27,28,29,30,31,32],"Prehabilitation","Preoperative Aerobic Training","Preoperative Care","Ovarian Cancer","Exercise Therapy","Postoperative Outcomes",[34,35,36,37,38,39],"postoperative outcomes","prehabilitation","nutritional support","psychological support","exercise therapy","ovarian cancer","NOT_YET_RECRUITING","2026-05-19",{"date":43,"type":44},"2026-05-27","ACTUAL",{"date":46,"type":21},"2026-05-14",{"date":48,"type":21},"2027-05-14",{"name":50,"class":51},"Jordan Leitch","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":60,"sex":61,"minAge":18,"maxAge":62,"enrollmentInfo":63,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":71,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":52},"100531832","diagnostic-efficacy-of-cnn-in-predicting-intraoperative-complications-and-postoperative-outcomes-in-smile-100531832","NCT06204926","Diagnostic Efficacy of CNN in Predicting Intraoperative Complications and Postoperative Outcomes in SMILE","Diagnostic Efficacy of Convolutional Neural Network Based Algorithm in Predicting Intraoperative Complications and Postoperative Outcomes in Small Incision Lenticule Extraction","Inclusion Criteria:\n\n* A condition in which the spherical equivalent refractive error of an eye is ≤-0.50 D when ocular accommodation is relaxed;\n* Age ≥18 years;\n* Spherical equivalent (SE) ≥-10.0D;\n* Corrected distance visual acuity (CDVA) ≥16\u002F20;\n* Stable myopia for at least 2 years;\n* No contact lenses wearing for at least 2 weeks.\n\nExclusion Criteria:\n\n* The presence or history of eye conditions other than myopia and astigmatism, such as keratoconus or external eye injury;\n* A history of eye surgery;\n* The presence or history of systemic diseases.",true,"ALL","45 Years",{"count":64,"type":21},1250,"OBSERVATIONAL","To evaluate the diagnostic efficiency of the neural network in predicting complications of Small Incision Lenticule Extraction in a multi-center cross-sectional study.",[68,69,70,32],"Deep Convolutional Neural Network","Small-incision Lenticule Extraction (SMILE) Surgery","Intraoperative Complications",[72,70,68,32],"femtosecond laser small-incision lenticule extraction","RECRUITING","2026-04-21",{"date":76,"type":44},"2026-04-24",{"date":78,"type":44},"2021-06-15",{"date":80,"type":21},"2027-12",{"name":82,"class":51},"Second Affiliated Hospital of Nanchang University",{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":4,"eligibilityCriteria":89,"healthyVolunteers":11,"sex":61,"minAge":18,"maxAge":4,"enrollmentInfo":90,"targetDuration":4,"studyType":65,"phases":4,"briefSummary":92,"conditions":93,"keywords":4,"overallStatus":73,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":52},"100592115","the-effect-of-perioperative-nutritional-care-on-recovery-after-knee-and-hip-replacement-surgery-100592115","NCT06989229","The Effect of Perioperative Nutritional Care on Recovery After Knee and Hip Replacement Surgery","Prospective Study on the Impact of Perioperative Nutritional Care in Patients Undergoing Total Knee and Hip Arthroplasty on Postoperative Outcomes","Inclusion Criteria:\n\nElective total hip replacement Elective total knee replacement\n\nExclusion Criteria:\n\nHip fracture Diabetes mellitus 1 Insulinotherapy",{"count":91,"type":21},1000,"This prospective observational study will assess the impact of standardized perioperative nutritional care on postoperative outcomes in patients undergoing elective total hip (THA) or knee arthroplasty (TKA) at the First Department of Orthopaedic Surgery, St. Anne's University Hospital in Brno. The protocol includes preoperative patient education, nutritional risk screening, and carbohydrate loading up to two hours before anesthesia, followed by early postoperative refeeding.\n\nData collection will include demographic and surgical variables, nutritional status, carbohydrate intake, and the occurrence of intra- and postoperative complications, including infection and delayed wound healing.\n\nAs perioperative nutritional care is part of routine clinical practice, the study requires no additional interventions or resources. Results will provide evidence on the effectiveness of structured nutritional support in enhancing recovery and reducing complications after joint replacement surgery.",[32,94,95],"Postoperative Complications","Length of Hospital Stay","2025-05-21",{"date":98,"type":44},"2025-05-25",{"date":100,"type":44},"2025-05-01",{"date":102,"type":21},"2027-12-31",{"name":104,"class":51},"St. Anne's University Hospital Brno, Czech Republic"]