[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"suture\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:suture":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,50,77,106],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100617720","antibiotic-coated-braided-suture-study-100617720",false,"NCT07322289","Antibiotic-coated Braided Suture Study","Evaluating the Use of Antibiotic-Coated Braided Sutures in Debridement, Antibiotic, and Implant Retention (DAIR) Procedures","Inclusion Criteria:\n\n* Age ≥18 years\n* Willing and able to provide informed consent\n* Primary Total Hip Arthroplasty or Total Knee Arthroplasty with Prosthetic Joint Infection Musculoskeletal Infection Society (MSIS) criteria\n* Prosthetic Joint Infection Treated with Debridement, Antibiotics, Implant Retention\n\nAcute Prosthetic Joint Infection: \\\u003C4 weeks since it was suspected\u002Fdiagnosed\n\nExclusion Criteria:\n\n* Staphylococcus aureus bacteremia\n* Mycobacterial, fungal, or parasitic infection\n* Concurrent infection needing prolonged Intravenous therapy\n* Septic shock\u002Fsystemic illness needing IV therapy\n* Patients with severe immunosuppression (ex: chemotherapy,\n\nneutropenia, HIV, steroid use\n\n* Allergy to Triclosan\n* Pregnancy\n* Prisoners","ALL","18 Years","89 Years",{"count":20,"type":21},142,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this study is to evaluate whether the use of antibiotic-coated (triclosan) braided sutures is non-inferior or potentially superior to standard monofilament sutures in patients with prosthetic joint infections (PJIs) managed with the DAIR protocol. Several studies in various surgical specialties have demonstrated the effectiveness and non-inferiority of triclosan-coated braided sutures in infected surgical cases, and the study intends to transpose this idea to the management of prosthetic joint infections. Monofilament sutures are the present standard of care in any infected joint case due their lower surface area for bacterial harborization, though surgeons sacrifice mechanical integrity and comfortability with the closure in the process. By demonstrating the safety of antibiotic -coated braided sutures, surgeons will no longer have to make this compromise.",[27,28,29,30,31],"Prosthetic Joint Infection","Debridement With Prosthesis Retention","Prosthetic Joint Infections of Hip","Prosthetic Joint Infections of Knee","Suture",[33,34,35,36],"prosthetic joint infection","debridement, antibiotics, implant retention","antibiotic coated braided sutures","monofilament suture","NOT_YET_RECRUITING","2026-03-18",{"date":40,"type":41},"2026-03-23","ACTUAL",{"date":43,"type":21},"2026-07-01",{"date":45,"type":21},"2027-12-31",{"name":47,"class":48},"University of Miami","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100611151","the-effect-of-hand-sewing-practices-on-suturing-skills-100611151","NCT07236853","The Effect of Hand Sewing Practices on Suturing Skills","The Effect of Hand Sewing Practices on Suturing Skills in Midwifery Students.","Inclusion Criteria:\n\n* Volunteers participating in the study,\n* Those taking the Normal Birth and Postpartum Term course for the first time,\n* Those who have not received suture training before,\n* Third-year midwifery students\n\nExclusion Criteria:\n\n* Students who are absent on the day the course is taught.",{"count":58,"type":21},83,[24],"The overall aim of this study was to evaluate the effects of hand-held suture exercises on non-locking continuous suture skills used in episiotomy repair in midwifery students. The study, conducted with a randomized, single-blind, controlled design, aimed to generate evidence of psychomotor skill transfer using Objective Structured Assessment of Technical Skills based performance scores and secondary indicators (time, number of errors, etc.).",[62,31,63],"Midwifery Education","Skill Performance",[65,31,66],"midwifery education","skill","2025-11-17",{"date":69,"type":41},"2025-11-19",{"date":71,"type":21},"2025-11-20",{"date":73,"type":21},"2025-12-31",{"name":75,"class":48},"Melek Şen Aytekin",2,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":4,"eligibilityCriteria":83,"healthyVolunteers":84,"sex":16,"minAge":17,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":22,"phases":88,"briefSummary":89,"conditions":90,"keywords":93,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":49},"100570018","optimizing-clinical-outcomes-in-caf--sctg-the-impact-of-compressive-sutures-100570018","NCT06701786","Optimizing Clinical Outcomes in CAF + SCTG: the Impact of Compressive Sutures","Compressive Sutures Improve Clinical Outcomes in CAF + SCTG for Treatment of RT1 Recessions\"","Inclusion Criteria:\n\n* systemic factors (no systemic diseases; no coagulation disorders; no medications affecting periodontal status in the previous 6 months; no pregnancy or lactation\n* never smokers\u002Fformer smokers \\>=10years\n* a full-mouth plaque score (FMPS)and a full-mouth bleeding score (FMBS) lower than 15%\n* no periodontal surgery on the experimental sites\n* \\>= 20 teeth without mobility\n* no presence of cervical carious lesions or periapical lesions at experimental sites\n* at least one RT1 buccal gingival recession\n\nExclusion Criteria:\n\n* systemic diseases\n* coagulation disorders\n* medications affecting periodontal status in the previous 6 months\n* pregnancy or lactation\n* Smokers",true,"80 Years",{"count":87,"type":21},40,[24],"This randomized controlled clinical trial aims to evaluate the additional effect on clinical outcomes of compressive sutures associated with coronally advanced flap (CAF) and subepithelial connective tissue graft (SCTG) for the treatment of RT1 gingival recessions (as classified by Cairo et al.).\n\nForty patients presenting with at least one RT1 recession will be enrolled in the study. Twenty participants will undergo CAF + SCTG with compressive sutures while the other 20 participants will receive the same procedure without compressive sutures. The primary outcome, complete root coverage (CRC), will be assessed six months after treatment.\n\nAdditional clinical parameters, including gingival recession (GR), clinical attachment level (CAL), pocket depth (PD), keratinized tissue width (KT), keratinized tissue thickness (GT), and Root Coverage Esthetic Score (RES), will be evaluated at baseline and at the six-month follow-up.\n\nPatient-reported outcomes (PROs) will also be measured, including the degree of general discomfort (D) experienced, assessed on a Visual Analog Scale (VAS) from 0 to 10, as well as patient-reported aesthetic satisfaction (PRES) and overall treatment satisfaction (OTS), both quantified on a VAS scale from 0 to 10.",[91,92,31],"Gingival Recessions","Gingival Recession, Mucogingival Surgery",[94,95,96,31],"Periodontal Plastic Surgery","Gingival recession","Coronally Advanced Flap","2024-11-19",{"date":99,"type":41},"2024-11-22",{"date":101,"type":21},"2024-12-01",{"date":103,"type":21},"2025-11-30",{"name":105,"class":48},"G. d'Annunzio University",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":112,"eligibilityCriteria":113,"healthyVolunteers":11,"sex":16,"minAge":114,"maxAge":115,"enrollmentInfo":116,"targetDuration":118,"studyType":119,"phases":4,"briefSummary":120,"conditions":121,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":131,"locationsCount":4},"100548810","virtual-reality-in-the-management-of-painful-or-anxiety-provoking-procedures-in-emergency-departments-100548810","NCT06425835","Virtual Reality in the Management of Painful or Anxiety-provoking Procedures in Emergency Departments","Virtual Reality in the Management of Painful or Anxiety-provoking Procedures in Emergency Departments: (Open Prospective Observational Study)","VR","Inclusion Criteria:\n\n* Patients aged 09 and 24 years\n* suturing a wound\n* changing a dressing\n* lumbar puncture,\n* peripheral venous line\n* blood test\n* intramuscular injection\n* reduction of a fracture\n* casting or plastering.\n\nExclusion Criteria:\n\n* impaired consciousness\n* epilepsy\n* wound\u002Finfection covering the helmet area\n* headache\n* intellectual\u002Fmental retardation\n* nausea, vomiting\n* patient already included in the protocol\n* pain requiring immediate medical attention. analgesic (VAS \\>5 and described as intolerable).","9 Years","24 Years",{"count":117,"type":21},300,"2 Years","OBSERVATIONAL","Study and evaluate the effectiveness of virtual reality in pain management.",[122,123,31],"Pain and Anxiety","Dislocation","2024-05-21",{"date":126,"type":41},"2024-05-22",{"date":128,"type":21},"2024-08-15",{"date":130,"type":21},"2026-12-15",{"name":132,"class":48},"University of Monastir"]