[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"same-day-discharge\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:same-day-discharge":91},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,51,76,107],{"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":30,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100479254","preoperative-oral-hydration-in-the-ambulatory-arthroplasty-population-100479254",false,"NCT05520593","Preoperative Oral Hydration in the Ambulatory Arthroplasty Population","Preoperative Oral Hydration in the Ambulatory Arthroplasty Population :A Single-Blinded Randomized Control Trial","Inclusion Criteria:\n\n* Candidates for ambulatory total knee arthroplasty\n* Candidates for ambulatory total hip arthroplasty\n* Candidates for ambulatory revision knee arthroplasty (liner exchange only)\n* Candidates for ambulatory revision hip arthroplasty (liner exchange only)\n* Case scheduled before noon (12 pm)\n* Patient agrees to same-day discharge and has a responsible adult to spend the night on the day of discharge\n\nExclusion Criteria:\n\n* BMI less than 18.5 or greater than 37.0\n* Patients with diabetes, chronic kidney disease, clotting disorders, or neurological conditions preventing control of the affected limb.\n* Pregnant women\n* Patients scheduled as ambulatory due to insurance mandates\n* Patients with a history of active ischemia, significant valvular disease, significant arrhythmias, obstructive sleep apnea as per Hospital for Special Surgery guidelines, chronic opioid dependence (chronic daily opioid use for six or more months), and glomerular filtration rate \\\u003C 60ml\u002Fmin.",true,"ALL","18 Years","75 Years",{"count":21,"type":22},312,"ESTIMATED","INTERVENTIONAL",[25],"NA","The purpose of this study is to investigate if the consumption of a complex carbohydrate drink preoperatively, decreases the length of stay and causes for failure to launch in patients undergoing ambulatory total joint arthroplasty.",[28,29],"Same-day Discharge","Length of Stay",[31,32,28,33,34,35,36,37],"Carbohydrate Drink","Perioperative Fluids","Total Joint Arthroplasty","Nausea","Vomiting","Same-day total hip arthroplasty","Same-day total knee arthroplasty","RECRUITING","2026-04-08",{"date":41,"type":42},"2026-04-13","ACTUAL",{"date":44,"type":42},"2022-11-07",{"date":46,"type":22},"2027-01",{"name":48,"class":49},"Hospital for Special Surgery, New York","OTHER",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":59,"enrollmentInfo":60,"targetDuration":4,"studyType":23,"phases":62,"briefSummary":63,"conditions":64,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100505187","is-physical-therapy-clearance-before-arthroplasty-home-discharge-necessary-100505187","NCT05858086","Is Physical Therapy Clearance Before Arthroplasty Home Discharge Necessary?","Is Postoperative Physical Therapy Clearance Necessary for Safe Home Discharge After Total Joint Arthroplasty?","PTClearSHoT","Inclusion Criteria:\n\n* are 18 years of age or older\n* undergo primary THA or TKA\n* are eligible for same-day home discharge (friends or family available to stay at home with the patient for one week postoperatively and medically stable for discharge from PACU per anesthesia).\n\nExclusion Criteria:\n\n* 90 years of age or older\n* have sleep apnea (not eligible for same-day discharge)\n* require overnight stay for any reason\n* undergo revision THA or TKA.","90 Years",{"count":61,"type":22},210,[25],"Conventionally, physical therapy (PT) clearance is sought before total joint arthroplasty (TJA) discharge. However, PT staffing limitations may preclude same-day discharge in patients having surgery late in the day. Failed same-day discharge in eligible TJA patients results in unnecessary hospital bed occupancy, which increases costs, limits operating room throughput for patients requiring inpatient admission, and introduces risks associated with longer length-of-stay.\n\nIn collaboration with an institutional PT department, the investigators developed a protocol for discharging same-day TJA patients without postoperative PT clearance. Immediately preoperatively, PT administers gait training. Patients are then discharged home after ambulating with post-anesthesia care unit (PACU) nurses trained by PT on postoperative mobilization. This allows for the maximum number of patients discharged home, including the last patient of the day, PT staffing limitations notwithstanding. Single-institution pilot data demonstrates no increased risk of falls, emergency room (ER) visits, or readmissions with this process.\n\nThe investigators propose a prospective, controlled, multicenter study to expand on pilot data. The study aim is to assess safety of day-of-surgery preoperative PT and postoperative ambulation with PACU nursing before TJA discharge. The primary endpoint is postoperative falls, while secondary endpoints include 90-day ER visits, 90-day hospital readmissions, patient-reported outcome measures, and patient satisfaction scores.",[65,33,28],"Physical Therapy","2026-02-06",{"date":68,"type":42},"2026-02-10",{"date":70,"type":42},"2024-09-27",{"date":72,"type":22},"2027-12",{"name":74,"class":49},"University of Maryland, Baltimore",2,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":11,"sex":84,"minAge":18,"maxAge":19,"enrollmentInfo":85,"targetDuration":4,"studyType":23,"phases":87,"briefSummary":88,"conditions":89,"keywords":93,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":106},"100610917","day-care-in-robotic-surgery-hysterectomy-investigate-quality-of-life-and-safety-with-same-day-discharge-after-robotic-hysterectomy-for-patients-with-benign-and-malignant-disease-a-multicenter-randomized-study-with-3-hospitals-in-stockholm-sweden-100610917","NCT07233811","Day Care in Robotic Surgery Hysterectomy. Investigate Quality of Life and Safety With Same Day Discharge After Robotic Hysterectomy for Patients With Benign and Malignant Disease. A Multicenter Randomized Study With 3 Hospitals in Stockholm Sweden.","DARSH - A Multicenter Randomized Controlled Trial: Day-care vs Overnight Stay in Robotic Assisted Hysterectomy in Patients With Bening Disease and Endometrial Cancer.","DARSH","Inclusion Criteria:\n\n* Patient that are planned to undergo total robotic hysterectomy with or without adnexal surgery at the three sites.\n* Both benign conditions and endometrial cancer.\n* All BMI groups and all uterus sizes.\n\nExclusion Criteria:\n\n* Age not over 75 years old,\n* No company at home first night after surgery\n* ASA class 3 that is not only because of high BMI.\n* Simultaneous prolapse surgery\u002Flymph node evacuation.\n* Severe endometriosis or patients with chronic pain conditions that have a special pain regimen after surgery.","FEMALE",{"count":86,"type":22},300,[25],"Patients undergoing robotic assisted hysterectomy in three different hospitals in Stockholm will be randomized to day-care (going home the same day as the surgery) or admission (staying at least one night after surgery). The aim with this study is to investigate if patients in day-care recover as fast\u002Ffaster as the other group that stays in the hospital. Both patients with benign disease and malign disease (endometrial cancer) will be included in the study.\n\nPatients quality of life (QoL) will be measured before surgery and after surgery at day 3,7 and 30 with a questionnaire called Eq-5D-5L from Euroqol. The questionnaire is validated for postoperative QoL and widely used.\n\nComplications due to surgery within the 30 first days after surgery will also be recorded in the two groups to make sure it is safe for the patients to go home the same day as their surgery.",[90,91,92],"Hysterectomy","Same Day Discharge","Robotic Surgical Procedures",[90,94,95,96],"Same day discharge","Robotic assisted Hysterectomy","Robotic suregery","2025-11-16",{"date":99,"type":42},"2025-11-18",{"date":101,"type":42},"2025-01-01",{"date":103,"type":22},"2028-01",{"name":105,"class":49},"Karolinska Institutet",3,{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":4,"eligibilityCriteria":113,"healthyVolunteers":16,"sex":114,"minAge":18,"maxAge":115,"enrollmentInfo":116,"targetDuration":4,"studyType":23,"phases":118,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":50},"100486954","phase-3-intra-operative-loop-diuretics-to-improve-same-day-discharge-rates-after-holep-100486954","NCT05620784","Intra-operative Loop Diuretics to Improve Same-day Discharge Rates After HoLEP","Loop Diuretics During Morcellation to Improve Same-day Discharge Rates After Holmium Laser Enucleation of the Prostate (HoLEP)","Inclusion Criteria:\n\n* Males 18 -89 undergoing HoLEP\n* Willing to sign the Informed Consent Form\n* Able to read, understand, and complete patient questionnaires.\n\nExclusion Criteria:\n\n* Allergy or hypersensitivity to furosemide or other loop diuretic\n* Anuric patients or patients with liver failure\n* Patients having a concurrent ureteroscopy +\u002F- laser lithotripsy, percutaneous nephrolithotomy, or non-urologic surgery at the time of their HoLEP\n* Anticipated need for perineal urethrostomy at the time of HoLEP\n* Patient not undergoing catheter removal and voiding trial at Northwestern Memorial Hospital","MALE","89 Years",{"count":117,"type":22},138,[119],"PHASE3","Holmium Laser Enucleation of the Prostate (HoLEP) is a size-independent treatment option for benign prostatic hypertrophy (BPH) as recommended by the American Urological Association (AUA) Guidelines. Loop diuretics (furosemide) have been given historically during the morcellation portion of HoLEP to promote urine production in the post-operative setting and to minimize the impact of fluid absorption during long periods of morcellation. The intra-operative use of 20mg IV furosemide in perioperative HoLEP pathways has been propagated with the dissemination of HoLEP across North America without evidence to support its routine administration. With increasing surgical efficiency from improvements in laser and morcellator technology, the role of intra-operative furosemide is unknown. This study is designed to assess if there is a significant difference in same day discharge rates after Holmium Laser Enucleation of the Prostate (HoLEP) with and without IV furosemide. .",[122,123,124,91],"BPH With Urinary Obstruction","BPH","Hematuria","2023-09-11",{"date":127,"type":42},"2023-09-13",{"date":129,"type":42},"2023-03-01",{"date":131,"type":22},"2024-08-01",{"name":133,"class":49},"Northwestern University"]