[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Riverside University Health System Medical Center\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":134},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,56,84,110],{"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":31,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":44,"lastUpdatePostDateStruct":45,"startDateStruct":48,"completionDateStruct":50,"leadSponsor":52,"locationsCount":55},"100646632","steri-strip-application-versus-standard-wound-closure-for-cesarean-section-incisions-100646632",false,"NCT07686913","Steri-Strip Application Versus Standard Wound Closure for Cesarean Section Incisions","A Randomized Prospective Trial Comparing Steri-Strip Application Versus Standard Wound Closure for Cesarean Section Incisions","STRIP-CS","Inclusion Criteria:\n\n* Female patients age 18 years or older\n* Pregnant patients undergoing cesarean delivery at Riverside University Health System Medical Center (RUHS)\n* Able and willing to provide informed consent\n\nExclusion Criteria:\n\n* Known allergy or hypersensitivity to Steri-Strip™ materials or adhesives\n* Inability or unwillingness to provide informed consent\n* Anticipated inability to complete the 30-day postpartum follow-up evaluation","FEMALE","18 Years",{"count":20,"type":21},610,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study is evaluating whether Steri-Strips® provide additional benefits when used after cesarean section (C-section) surgery. Steri-Strips are adhesive strips that are commonly placed over a surgical incision to provide support while the wound heals. At our hospital, Steri-Strips are routinely used after C-sections in addition to standard wound closure techniques, although they are not considered part of the standard recommended closure method.\n\nResearchers want to determine whether adding Steri-Strips actually reduces wound complications such as infection, fluid collection under the skin, or reopening of the incision. Previous studies have shown mixed results, with some suggesting little difference in wound healing outcomes while others reported differences in scar appearance. Steri-Strips may also increase costs, add time to the surgery, and occasionally cause skin irritation or allergic reactions.\n\nParticipants in this study will be randomly assigned to one of two groups. One group will receive standard cesarean wound closure with Steri-Strips, while the other group will receive standard wound closure without Steri-Strips. Researchers will compare wound healing, complications, patient outcomes, and costs between the two groups.\n\nThe goal of this study is to determine whether Steri-Strips improve recovery after cesarean delivery and whether their routine use is beneficial and cost-effective. The findings may help guide future recommendations for cesarean wound care and improve outcomes for patients undergoing C-section delivery.",[27,28,29,30],"Cesarean Section","Surgical Site Infection","Wound Dehiscence","Seroma",[27,32,33,34,35,36,28,29,30,37,38,39,40,41,42],"Cesarean Delivery","C-Section","Steri-Strips","Skin Closure","Wound Closure","Postoperative Wound Complications","Obstetric Surgery","Incision Management","Surgical Wound Healing","Maternal Morbidity","Randomized Controlled Trial","RECRUITING","2026-06-29",{"date":46,"type":47},"2026-07-07","ACTUAL",{"date":49,"type":21},"2026-06",{"date":51,"type":21},"2027-12",{"name":53,"class":54},"Riverside University Health System Medical Center","OTHER",1,{"id":57,"slug":58,"hasResults":11,"nctId":59,"briefTitle":60,"officialTitle":60,"acronym":4,"eligibilityCriteria":61,"healthyVolunteers":11,"sex":62,"minAge":18,"maxAge":4,"enrollmentInfo":63,"targetDuration":4,"studyType":22,"phases":65,"briefSummary":68,"conditions":69,"keywords":72,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":55},"100609960","phase-2-enteral-vancomycin-as-primary-prophylaxis-against-clostridioides-difficile-infection-in-critically-ill-patients-100609960","NCT07221370","Enteral Vancomycin as Primary Prophylaxis Against Clostridioides Difficile Infection in Critically Ill Patients","Inclusion Criteria:\n\n1. Must meet all 3 criteria:\n\n   * Adults aged 18 years and older.\n   * Receiving ≥ 72 hours of a systemic antibiotic during index hospitalization.\n   * Admitted ≥ 72 hours into their index hospitalization.\n2. And must meet 2 additional of the following high-risk criteria\n\n   * Age ≥ 65 years\n   * Previous residence in long-term care facility\n   * Previous proton pump inhibitor use (chronic or as needed)\n   * Inflammatory bowel disease\n   * Immunocompromised state (HIV\u002FAIDS; transplant recipient; receipt of prednisone 20 mg daily for at least one month, immunosuppressants, or chemotherapy)\n   * End stage renal disease (ESRD)\n   * Diabetes mellitus\n   * Receipt of catecholamines (norepinephrine at a rate of ≥ 5 mcg\u002Fmin)\n   * Hospitalized ≤ 30 days prior to the index hospitalization.\n   * Received systemic antibiotics during that prior hospitalization.\n\nExclusion Criteria:\n\n* Pregnant or breastfeeding women\n* Currently incarcerated individuals\n* Individual or legal representative whose informed consent cannot be obtained\n* Subject not expected to survive the ICU stay or subject likely to be considered for palliative or hospice care\n* Receiving concurrent treatment with metronidazole for any indication\n* One-time empiric use of metronidazole is allowed and does not constitute an exclusion criterion\n* Receiving concurrent probiotics\n* Allergic reaction or had a contraindication for use of enteral vancomycin\n* History of prior CDI within the past 90 days of randomization\n* Had suspected active CDI prior to inclusion\n* Infection requiring more than 14 21 days of systemic antibiotics during index hospitalization","ALL",{"count":64,"type":21},176,[66,67],"PHASE2","PHASE3","The goal of this clinical trial is to determine if oral vancomycin can prevent C.diff infection in adults who are critically ill and are at high risk of C.diff infection due to their medical conditions and being in the hospital. It will also help us learn about the safety of the drug in this setting. The main questions the trial aims to answer are:\n\n* Does oral vancomycin lower the rate of C.diff infection in high-risk patients?\n* Does C.diff carrier status change the C.diff infection rate as well as clearance of carrier status when vancomycin is used as primary prophylaxis? Researchers will compare the oral, active drug vancomycin to a placebo (a look-alike substance that contains no drug) to determine if vancomycin works to prevent C.diff infection in the hospital.\n\nParticipants will:\n\n* Take oral vancomycin or a placebo while they receive systemic antibiotic(s) for up to five days after the last dose of said systemic antibiotic(s). The treatment of said systemic antibiotic(s) is not to exceed 21 days.\n* When discharged from the hospital, participants will continue to take the study medication in the event he\u002Fshe did not complete the intended course of the study medication while in the hospital.\n* Participants will provide stool sample or rectal swabs for to assess their C.diff carrier status as well as any change in stool microbiome status, including VRE (vancomycin resistant Enterococcus)\n* After completion of the intervention period, participants will be contacted via telephone to assess if they developed diarrhea or any untoward effects of study medication.",[70,71],"Clostridium Difficile Infection","Vancomycin Resistant Enterococci Infection",[73,74,75],"Clostridium difficle infection","primary prophylaxis","Vancomycin resistant enterocci infection","2025-11-05",{"date":78,"type":47},"2025-11-10",{"date":80,"type":47},"2024-10-21",{"date":82,"type":21},"2026-12-31",{"name":53,"class":54},{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":62,"minAge":4,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":93,"phases":4,"briefSummary":94,"conditions":95,"keywords":99,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":4},"100580968","postoperative-delirium-after-intraoperative-ephedrine-versus-norepinephrine-100580968","NCT06844201","Postoperative Delirium After Intraoperative Ephedrine Versus Norepinephrine","Postoperative Delirium After Intraoperative Ephedrine Versus Norepinephrine: a Retrospective TriNetX Database Study","Ephedrine group:\n\nInclusion Criteria:\n\n* underwent surgery (CPT code 1003143)\n* administered ephedrine on the day of surgery\n\nExclusion Criteria:\n\n* received both vasopressors (ephedrine and norepinephrine) on the day of surgery.\n* patients who underwent neurology and neuromuscular surgery, cardiac surgery, and cardiac procedures\n* patients who were administered epinephrine or dopamine on the day of surgery\n* patients who were administered ephedrine or norepinephrine at any time within the 7 days following the day of surgery\n* a prior history of disorientation (ICD-10 code R41.0) or unspecified dementia (F03)\n\nNorepinephrine group:\n\nInclusion Criteria:\n\n* underwent surgery (CPT code 1003143)\n* administered norepinephrine on the day of surgery\n\nExclusion Criteria:\n\n* received both vasopressors (ephedrine and norepinephrine) on the day of surgery.\n* patients who underwent neurology and neuromuscular surgery, cardiac surgery, and cardiac procedures\n* patients who were administered epinephrine or dopamine on the day of surgery\n* patients who were administered ephedrine or norepinephrine at any time within the 7 days following the day of surgery\n* a prior history of disorientation (ICD-10 code R41.0) or unspecified dementia (F03)",{"count":92,"type":21},10000,"OBSERVATIONAL","This retrospective study aims to investigate the effects of norepinephrine compared to ephedrine, administered on the day of surgery, on the incidence of postoperative delirium.",[96,97,98],"Ephedrine","Norepinephrine","Postoperative Delirium (POD)",[96,97,100],"Postoperative delirium","NOT_YET_RECRUITING","2025-02-19",{"date":104,"type":47},"2025-02-25",{"date":106,"type":21},"2025-02-20",{"date":108,"type":21},"2025-08-01",{"name":53,"class":54},{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":62,"minAge":18,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":22,"phases":119,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":101,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":55},"100572730","low-pressure-pneumoperitoneum-using-airseal-for-reduction-in-postoperative-shoulder-pain-following-robot-assisted-hiatal-hernia-repair-100572730","NCT06737068","Low Pressure Pneumoperitoneum Using AirSeal® for Reduction in Postoperative Shoulder Pain Following Robot Assisted Hiatal Hernia Repair","Low Pressure Pneumoperitoneum Using AirSeal® for Reduction in Postoperative Shoulder Pain Following Robot Assisted Hiatal Hernia Repair: a Prospective Randomized Controlled Trial.","Inclusion Criteria:\n\n* patients undergoing elective robot assisted hiatal hernia repair\n\nExclusion Criteria:\n\n* patients less than 18 years of age\n* conversion to open surgery\n* BMI \\> 40\n* history of abdominoplasty\n* history of chronic pain and\u002For opioid dependence\n* history of COPD and\u002For supplemental oxygen use\n* pregnant patients\n* incarcerated patients\n* patient refusal",{"count":118,"type":21},120,[24],"The goal of this clinical trial is to evaluate the incidence and severity of post-operative shoulder pain following elective robot-assisted hiatal hernia repair in hopes of reducing pain and associated costs as well as clinic and emergency department visits due to this pain. You will undergo standard robot-assisted hiatal hernia repair with the standard postoperative care. The only difference is that you may be selected for the group where lower pressures used to fill your abdomen with carbon dioxide will be used, and you will be asked to fill out logs regarding your pain postoperatively. You will have postoperative appointments that are standard following this procedure.",[122,123,124,125],"Hernia, Hiatal","Pneumoperitoneum","Postoperative Pain","Shoulder Pain","2024-12-11",{"date":128,"type":47},"2024-12-17",{"date":130,"type":21},"2025-01-01",{"date":132,"type":21},"2027-01",{"name":53,"class":54},""]