[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Slagelse Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":137},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,77,105],{"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":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100635222","the-spotlight-study-early-identification-of-post-surgical-infections-using-bedside-ultrasound-100635222",false,"NCT07549880","The Spotlight Study: Early Identification of Post-Surgical Infections Using Bedside Ultrasound.","Post-Laparotomy Fluid Monitoring With Point of Care Ultrasonography : Predicting Surgical Site Infection & Optimizing Patient Convalescence (SPOTLIGHT Study).","SPOTLIGHT","Inclusion Criteria:\n\n* Adults \\>18 years.\n* Undergoing emergency or elective laparotomy.\n* Primary or delayed primary wound closure (DPC).\n* Wound classification: clean, clean-contaminated, contaminated, or dirty.\n* Informed consent obtained.\n\nExclusion Criteria:\n\n* Laparoscopic surgery\n* Wounds healing by secondary intention.\n* Ongoing wound dehiscence treatment with Negative Pressure Wound Therapy (NPWT).\n* Non-Danish residents","ALL","18 Years",{"count":20,"type":21},100,"ESTIMATED","INTERVENTIONAL",[24],"NA","Introduction:\n\nThe goal of this observational study is to learn whether point-of-care ultrasound (POCUS) can help detect early fluid build-up under the skin after open abdominal surgery (laparotomy) and whether these findings can predict surgical site infection. The study includes adults who recently had emergency or planned open abdominal surgery.\n\nHypothesis:\n\nThe main questions it aims to answer are:\n\n1. Does ultrasound identify subcutaneous fluid collections early after surgery?\n2. Do these fluid collections help predict which participants will develop a surgical site infection?\n\nIntervention:\n\nParticipants will:\n\n1. Have a superficial wound swab taken once at the start of the study (for research only).\n2. Receive three ultrasound scans of their surgical wound during days 1-3, 4-6, and 7-9 after surgery.\n3. Have their wound checked for redness, swelling, tenderness, or discharge before each scan.\n4. Be followed for 7 and 30 days after surgery (and up to 90 days if they have implanted mesh) to see whether an infection develops.\n\nUltrasound is non-invasive and safe. According to the protocol, \"no serious adverse effects are expected,\" though some participants may feel brief discomfort from pressure on a tender wound.\n\nThis study will help researchers understand whether routine bedside ultrasound can support earlier detection of wound infections and improve postoperative care in the future.",[27,28,29],"Surgical Site Infection (SSI)","Emergency Laparotomies","Point of Care Ultrasound (POCUS)",[31,32,33],"point of care ultrasound (POCUS)","surgical site infection (SSI)","Emergency laparotomies","RECRUITING","2026-04-17",{"date":37,"type":38},"2026-04-24","ACTUAL",{"date":40,"type":38},"2026-04-10",{"date":42,"type":21},"2027-08-30",{"name":44,"class":45},"Slagelse Hospital","OTHER",3,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":61,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":76},"100539139","supervised-exercise-based-rehabilitation-for-people-with-intermittent-claudication-in-denmark-100539139","NCT06299956","Supervised Exercise-based Rehabilitation for People With Intermittent Claudication in Denmark","Supervised Exercise-based Rehabilitation for People With Intermittent Claudication - Study Protocol for a Danish Implementation Process (StRiDE).","StRiDE","Inclusion criteria:\n\n* Relevant symptoms of intermittent claudication; leg pain when walking due to arteriosclerosis and relieve of symptoms during rest.\n* Distal blood pressure with an ankle-brachial index (ABI) \\> 50 mmHg for non-diabetics or toe brachial index (TBI) \\> 40 mmHg for diabetics.\n\nExclusion criteria:\n\n• Evaluated by a vascular surgeon: patients with contraindications e.g. medical issues or comorbidity that enables a participation in SET are not referred.",{"count":56,"type":21},600,[24],"The goal of this project is to implement a protocol for a supervised exercise therapy intervention including smoking cessation in the municipalities in region Zealand in Denmark. The participants are adults with intermittent claudication.\n\nThe objective of this project is to describe:\n\n1. The development and design of the implementation process of a rehabilitative intervention including SET and smoking cessation in Region Zealand with a 6-month follow-up period after completion of the SET.\n2. The ongoing quality monitoring process of the implementation in terms of referral, recruitment, retention, data completeness, intervention delivery and attendance and to collect feedback that will guide refinements of the intervention delivery and data collection.\n3. Outcomes available for assessment of benefits and harms from the SET intervention.\n\nParticipants will be asked to do supervised exercise therapy by walking on a treadmill for 3 times a week for 12 weeks, and engage in smoking cessation, if they are smoking.",[60],"Intermittent Claudication",[62,63,64,65,66,67],"Exercise therapy","Smoking cessation","Implementation","Stakeholders","Walking","Treadmill","2025-05-20",{"date":70,"type":38},"2025-05-25",{"date":72,"type":38},"2023-09-01",{"date":74,"type":21},"2029-01",{"name":44,"class":45},1,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":84,"minAge":85,"maxAge":86,"enrollmentInfo":87,"targetDuration":4,"studyType":89,"phases":4,"briefSummary":90,"conditions":91,"keywords":93,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":76},"100506243","get-the-benefits-from-the-start-improving-breastfeeding-100506243","NCT05871853","Get the Benefits From the Start. Improving Breastfeeding","Getting the Benefits From the Beginning. Improving Breastfeeding Support for Families at Risk of Breastfeeding Difficulties","Inclusion Criteria:\n\n* All women giving birth at Slagelse Hospital and their infants during the study period\n* Age at 15 years and above\n\nExclusion Criteria:\n\n* families with a planned placement of the infant in a fostercare","FEMALE","15 Years","100 Years",{"count":88,"type":21},1600,"OBSERVATIONAL","Breastfeeding is beneficial for the physical and mental health of mothers and infants alike.\n\nMost new mothers in Denmark intend to breastfeed, however, a substantial proportion do not succeed to breastfeed as intended.\n\nIn Region Zealand, few women breastfeed than in the rest of Denmark in which may be related to a higher proportion of women being overweight, having socio-economic constraints and a low educational level, all associated with breastfeeding difficulties. There is limited knowledge on how to deliver a tailored support aimed at families at high risk of breastfeeding difficulties in a high-income country.\n\nWe plan to conduct a study aiming to strengthen breastfeeding support to families at risk of breastfeeding difficulties, delivering at Slagelse Hospital, across healthcare sectors, including obstetric and neonatal departments, primary care and civil society.\n\nThe study aims to develop, implement, and evaluate a supportive breastfeeding intervention with specific focus on families at high risk of complicated breastfeeding and early breastfeeding cessation - a prospective cohort study in Region Zealand, Denmark.\n\nPotentially, results can help reducing inequality in health thus more families achieve exclusive breastfeeding and gain health benefits from breastfeeding",[92],"Breastfeeding",[92,94,95,96],"Infant","Newborn","Post-natal Care","2023-06-15",{"date":99,"type":38},"2023-06-18",{"date":101,"type":38},"2023-05-25",{"date":103,"type":21},"2028-12-31",{"name":44,"class":45},{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":11,"sex":17,"minAge":112,"maxAge":113,"enrollmentInfo":114,"targetDuration":4,"studyType":22,"phases":116,"briefSummary":117,"conditions":118,"keywords":124,"overallStatus":129,"whyStopped":4,"lastUpdateSubmitDate":130,"lastUpdatePostDateStruct":131,"startDateStruct":132,"completionDateStruct":134,"leadSponsor":136,"locationsCount":4},"100508613","isotonic-saline-for-children-with-bronchiolitis-100508613","NCT05902702","Isotonic Saline for Children With Bronchiolitis","Isotonic Saline for Children With Bronchiolitis - a Randomized Controlled Non-inferiority Trial","Inclusion Criteria:\n\n* Children aged 0-12 months, whose parents give informed consent to participate, with symptoms of bronchiolitis including at least one of:\n\n  * Runny nose\n  * Dry and persistent cough\n  * Labored breathing (tachypnea, retractions, nasal flaring)\n  * Grunting\n  * Cyanosis or apnea\n  * Wheezing or crackles on auscultation\n  * O2 saturations below 92 %\n  * Difficulties feeding\n\nExclusion Criteria:\n\n* Children with cystic fibrosis or other serious congenital lung diseases\n* Children in whom treatment with short-acting beta-2 agonist is initiated (as this is delivered in nebulized isotonic saline).","1 Day","12 Months",{"count":115,"type":21},300,[24],"The goal of this randomized clinical trial is to investigate the optimal supportive treatment of bronchiolitis in infants from 0-12 months of age. The main question\\[s\\] it aims to answer are:\n\n* To investigate whether isotonic saline should be used as supportive treatment for children with bronchiolitis, and if so, identify the optimal route of administration. The primary outcome is duration of hospitalization.\n* To investigate the current epidemiology of the viral pathogens causing bronchitis in children in Denmark, and to assess whether children infected with specific pathogens might benefit from treatment with isotonic saline.\n\nThe children are randomized after inclusion through computer randomization to one of the 3 arms in the study:\n\n1. Nebulized isotonic saline\n2. Nasal irrigation with isotonic saline\n3. No treatment with saline\n\nThe investigators will compare treatment with saline (both methods) with no treatment, and the investigators will also compare the two methods of delivery of saline (nebulized vs. nasal irrigation).",[119,120,121,122,123],"Bronchiolitis","Respiratory Disease","Asthma in Children","Viral Infection","Acute Respiratory Infection",[125,126,127,128],"Nebulized saline","Nasal saline drops","Nasal saline irrigation","Respiratory severity score","NOT_YET_RECRUITING","2023-06-13",{"date":97,"type":38},{"date":133,"type":21},"2023-09",{"date":135,"type":21},"2029-09",{"name":44,"class":45},""]