[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"United States Naval Medical Center, Portsmouth\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":104},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,73],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100592217","cast-art-for-kids-with-extremity-fractures-100592217",false,"NCT06990555","Cast Art for Kids With Extremity Fractures","Cast Art for Kids With Extremity Fractures on Satisfaction and Perception of Pain (CAKEPOP)","CAKE POP","Inclusion Criteria:\n\n* Age 5 years old and greater, and less than 18 years old\n* Sustained an upper or lower extremity fracture\n* Scheduled for orthopedic clinic visit for injury evaluation\n* Have radiographic and clinical data available for review\n\nExclusion Criteria:\n\n* Age 18 years old or greater at the time of screening\n* Patient\u002Fparents do not consent to being included in the study\n* Underwent surgery",true,"ALL","5 Years","18 Years",{"count":22,"type":23},96,"ESTIMATED","INTERVENTIONAL",[26],"NA","The goal of this clinical trial is to compare casts with cast art versus those without art in children who sustain a fracture of the extremity. The main goals are:\n\n* Determine the difference in satisfaction as measured by the visual analog scale for satisfaction between patients treated in a cast with cast customization versus those in a cast with no cast art\n* Determine the difference in perceived pain scores between patients treated in a cast with cast customization versus those in a case with no cast art\n\nParticipants will be randomized to one of three groups: one with plain white cast, one with cast of color wrap of choice, and one with custom cast art.\n\nResearchers will compare to see the differences in satisfaction and perception of pain based on what cast the study participant receives.",[29],"Fractures, Bone",[31,32,33],"Cast","Art","Fractures","RECRUITING","2025-10-07",{"date":37,"type":38},"2025-10-09","ACTUAL",{"date":40,"type":38},"2023-05-08",{"date":42,"type":23},"2025-12-30",{"name":44,"class":45},"United States Naval Medical Center, Portsmouth","FED",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":17,"sex":53,"minAge":20,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":46},"100553585","phase-2-preoperative-use-of-pantoprazole-for-prevention-of-post-operative-nausea-and-vomiting-in-gynecologic-surgery-100553585","NCT06488001","Preoperative Use of Pantoprazole for Prevention of Post Operative Nausea and Vomiting in Gynecologic Surgery","Inclusion Criteria:\n\n* Undergoing elective gynecological surgery by either an open abdominal or minimally invasive approach (to include both endoscopic and vaginal). Procedure must be performed under general anesthesia.\n\nExclusion Criteria:\n\n* Pregnant,\n* Patients with gastrointestinal disease requiring ongoing medical management.\n* Prior gastrointestinal surgery with the exception of diagnostic procedures, appendectomy and cholecystectomy.\n* Patients with a history of H2 receptor blocker use, proton pump inhibitor use or other GERD specific therapy within 30 days of surgery.\n* Any patient identified by their surgical care team as having a history of PONV warranting additional perioperative prophylaxis.\n* Known r suspected malignancy\n* Lactose intolerance","FEMALE","79 Years",{"count":56,"type":23},132,[58],"PHASE2","The goal of this clinical trial is to see if pantoprazole (a proton pump inhibitor used for acid reflux\u002Fheart burn) can reduce nausea and vomiting after gynecologic surgery in women between the ages of 18 and 79.\n\nResearchers will compare a placebo to the active medication.\n\nParticipants will be asked to take three pills around their surgery, two taken before and one taken the night after.",[61],"Postoperative Nausea and Vomiting",[63,64],"PONV","Postoperative nausea","2025-05-16",{"date":67,"type":38},"2025-05-21",{"date":69,"type":38},"2022-08-26",{"date":71,"type":23},"2026-12",{"name":44,"class":45},{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":17,"sex":18,"minAge":20,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":24,"phases":82,"briefSummary":84,"conditions":85,"keywords":87,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":46},"100535502","phase-4-liposomal-bupivacaine-vs-bupivacaine-with-dexmedetomidine-in-erector-spinae-plane-blocks-for-mastectomies-100535502","NCT06252662","Liposomal Bupivacaine Vs Bupivacaine with Dexmedetomidine in Erector Spinae Plane Blocks for Mastectomies","Liposomal Bupivacaine Vs Bupivacaine with Dexmedetomidine in an Erector Spinae Plane Block for Mastectomies in Cancer Patients: a Randomized Control Trial","Inclusion Criteria:\n\n* Patients requiring any variation of mastectomy with or without axillary lymph node dissection.\n* Patient agrees to a peripheral nerve block.\n* Patient agrees to be a study participant.\n* APS team believes a peripheral nerve block would be appropriate for the patient after reviewing medical\u002Fsurgical history.\n* Surgeon agrees with the block plan by APS.\n\nExclusion Criteria:\n\n* Patient declines a peripheral nerve block.\n* Patient declines to be a study participant.\n* APS team believes a peripheral nerve block is not clinically indicated.\n* Surgeon does not want a peripheral nerve block.\n* Patient has allergy to local anesthestic.\n* Patient has an active infection at the site of the peripheral nerve block.\n* Patient with pre-existing neural deficits along the distribution of the block.\n* Patient with coagulopathy.\n* Patient taking antithrombotic drugs outside the ASRA guidelines.\n* Patients weight is less that 50 kg due to concerns for local anesthetic toxicity syndrome.",{"count":81,"type":23},200,[83],"PHASE4","Perform a comparison of effective pain relief duration between liposomal bupivacaine and dexmedetomidine when added to bupivacaine in a block for mastectomy for cancer surgery. The erector spinae plane block is a well-established block that is utilized for post operative pain control for procedures performed on the soft tissue of the chest and chest wall as well as intrathoracic procedures. The goal is comparison of the effective duration of both study groups to determine if there is a significant difference in time and amount of post operative opioids required which admitted to hospital.",[86],"Breast Cancer",[88,89,90,91,92,93,94,95],"erector spinae plane block","bupivacaine","morphine equivalents","pain score","post-operative pain","post-surgical pain","liposomal bupivacaine","Exparel","2024-11-15",{"date":98,"type":38},"2024-11-19",{"date":100,"type":38},"2024-10-15",{"date":102,"type":23},"2025-10",{"name":44,"class":45},""]