[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"vascular-access-device-complications\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:vascular-access-device-complications":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100632105","comparing-basilic-and-cephalic-vein-approaches-for-midline-catheter-placement-in-children-100632105",false,"NCT07509359","Comparing Basilic and Cephalic Vein Approaches for Midline Catheter Placement in Children","Comparing Basilic and Cephalic Vein Approaches for Midline Catheter Placement in Children: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Age 2-17 years undergoing general anesthesia\n* Midline catheter placement deemed necessary by attending anesthesiologist (≥1 of: expected ≥2 postop blood draws; expected blood loss ≥40% EBV; continuous antibiotic therapy; hospitalization ≥7 days; surgical team request)\n\nExclusion Criteria:\n\n* Need for central venous catheter per surgical team\n* Coagulopathy\n* History of severe thrombosis\n* Other investigator-determined ineligibility",true,"ALL","2 Years","17 Years",{"count":21,"type":22},96,"ESTIMATED","INTERVENTIONAL",[25],"NA","This prospective randomized controlled trial aims to compare basilic vein and cephalic vein approaches for midline catheter placement in pediatric patients undergoing general anesthesia. Participants aged 2 to 17 years who require midline catheter insertion will be randomly assigned 1:1 to either the basilic vein group or the cephalic vein group. The primary outcome is the clinical blood sampling success rate during the catheter dwell period, defined as successful aspiration of ≥2 mL of blood through the midline catheter at least once without additional venipuncture. Secondary outcomes include operator-rated difficulty, number of puncture attempts, first attempt cannulation success rate, vein diameter and depth, catheter dwell time, catheter-related complications, and patient satisfaction. A total of 96 participants (48 per arm) will be enrolled at Seoul National University Children's Hospital.",[28],"Vascular Access Device Complications","RECRUITING","2026-03-29",{"date":32,"type":33},"2026-04-03","ACTUAL",{"date":35,"type":22},"2026-04-01",{"date":37,"type":22},"2030-04-01",{"name":39,"class":40},"Seoul National University Hospital","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":17,"minAge":50,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":23,"phases":53,"briefSummary":54,"conditions":55,"keywords":59,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":4},"100598060","evaluating-the-effect-of-the-valsalva-maneuver-on-invasive-pain-during-arteriovenous-fistula-cannulation-in-hemodialysis-patients-100598060","NCT07066579","Evaluating the Effect of the Valsalva Maneuver on Invasive Pain During Arteriovenous Fistula Cannulation in Hemodialysis Patients","Evaluation of the Effect of the Valsalva Maneuver on Invasive Pain During Arteriovenous Fistula Cannulation in Hemodialysis Patients","VALPAIN-HD","Inclusion Criteria:\n\n* Age 18 years or older\n* Receiving hemodialysis treatment via arteriovenous fistula for at least 3 months\n* No analgesic medication use within the past 24 hours\n* Systolic blood pressure between 90-160 mmHg and diastolic between 60-100 mmHg\n* Pain score ≥ 1 on Visual Analogue Scale during AVF cannulation\n* Able to perform the Valsalva maneuver (no contraindications)\n* No communication barriers or severe psychiatric disorders\n* Provided written informed consent\n\nExclusion Criteria:\n\n* Unable to correctly perform the Valsalva maneuver\n* Failed first cannulation attempt\n* History of acute myocardial infarction or malignant arrhythmia\n* Aneurysm, infection, edema, or scar tissue at AVF site\n* Pregnancy\n* Voluntary withdrawal from the study at any stage\n* Switching dialysis centers or requiring hospitalization during the study","18 Years",{"count":52,"type":22},60,[25],"The goal of this clinical trial is to evaluate whether the Valsalva maneuver reduces invasive pain during arteriovenous fistula (AVF) cannulation in adult hemodialysis patients. The main questions it aims to answer are:\n\nDoes the Valsalva maneuver effectively reduce pain intensity during AVF cannulation as measured by the Visual Analogue Scale (VAS)?\n\nIs the Valsalva maneuver feasible, acceptable, and satisfactory for patients, and can it be sustainably implemented over multiple sessions?\n\nResearchers will compare patients performing the Valsalva maneuver (intervention group) with those receiving standard care without any intervention (control group) to see if pain scores are significantly lower and whether patients are willing to continue using this technique voluntarily.\n\nParticipants will:\n\nReceive training and supervised practice on the Valsalva maneuver before inclusion in the study\n\nPerform the Valsalva maneuver during AVF cannulation in each hemodialysis session for 12 sessions\n\nComplete VAS pain assessments after each session\n\nComplete a patient satisfaction and feasibility form at the end of the study",[56,57,58,28],"Arteriovenous Fistula","Pain","Hemodialysis Access Failure",[60,56,61,62],"Hemodialysis","Cannulation Pain","Valsalva Maneuver","NOT_YET_RECRUITING","2025-07-05",{"date":66,"type":33},"2025-07-15",{"date":68,"type":22},"2025-09-01",{"date":70,"type":22},"2026-09-01",{"name":72,"class":40},"Cansu POLAT DÜNYA"]