[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"alveolar-osteitis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:alveolar-osteitis":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,71],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100628414","surgeons-prediction-of-dental-surgery-complications-and-the-influence-of-patient-characteristics-development-of-an-ai-model-100628414",false,"NCT07461324","Surgeons' Prediction of Dental Surgery Complications and the Influence of Patient Characteristics: Development of an AI Model","Systematic Risk Assessment Prior to Oral Surgery","Inclusion Criteria:\n\n* Patients reffered from a general dentist practicioner for the following surgeries: third molar removal, apicoectomy, dental implant placement.\n* Patients \\>15 years of age\n* A valid diagnosis prior to the surgery\n* Cases with fully completed questionnaires.\n\nExclusion Criteria\n\n* Pathological condition requiring hospital refferal\n* Complications following re-surgery\n* Re-assesment of the diagnosis from the general dentist practicioner\n\nSpecific for apical surgery:\n\n* Root fracture present.\n* Buccal bone height \\\u003C3mm.\n\nSpecific for third molar removal:\n\n\\- if coronectomy is conducted instead of total root removal.\n\nSpecific for dental implant:\n\n* if an implant has been placed before in the same region of interest.\n* Health conditions were dental implants are contraindicated.",true,"ALL","15 Years",{"count":20,"type":21},3000,"ESTIMATED","1 Year","OBSERVATIONAL","The goal of this observational study is to learn how to better predict and prevent intra- and postoperative complications in oral surgery in adult patients referred for oral surgical procedures. The study aims to understand how accurately surgeons can foresee complications and which patient, tooth, and surgery related factors influence the outcomes.\n\nThe research questions are:\n\n* What is the incidence of intra and postoperative complications in oral surgery?\n* Which factors predict these complications, and how accurately can surgeons anticipate them?\n* Can the development of an AI tool reduce postoperative complications?\n\nParticipants will:\n\n* Receive standard oral surgery treatment at a private referral clinic (Specialtandlægerne Sjælland).\n* Have clinical information collected about their procedure, medical history, and personal characteristics (including anxiety level).\n* Conduct a short questionnaire, the STAI-6 and the I-PANAS-SF.\n* Have the surgeon record their prediction of whether complications are expected.\n* Be followed in the postoperative lapse to document whether complications occur after surgery.",[26,27,28,29,30,31,32],"Postoperative Infections","Mandibular Nerve Injuries","Alveolar Osteitis","Complication","Dental Implantation","Tooth Extraction","Apical Surgery","NOT_YET_RECRUITING","2026-03-04",{"date":36,"type":37},"2026-03-10","ACTUAL",{"date":39,"type":21},"2026-04-01",{"date":41,"type":21},"2030-06-01",{"name":43,"class":44},"University of Copenhagen","OTHER",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":16,"sex":17,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":58,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100601118","assessment-of-ozone-therapy-for-management-of-post-extraction-localized-alveolar-osteitis-100601118","NCT07106333","Assessment of Ozone Therapy for Management of Post-Extraction Localized Alveolar Osteitis","Management of Post-Extraction Localized Alveolar Osteitis","Inclusion Criteria:\n\nAge: 18-60 years.\n\nPatients undergoing simple (non-surgical) extractions.\n\nMedically healthy individuals.\n\nExclusion Criteria:\n\nPatients already treated for AO.\n\nPresence of systemic diseases affecting healing.\n\nSevere infections or facial swelling.\n\nIncomplete follow-up.\n\nContraindications to ozone therapy: G6PD deficiency, hyperthyroidism, malignant hypertension, recent myocardial infarction.","20 Years","50 Years",{"count":56,"type":21},40,"INTERVENTIONAL",[59],"NA","This clinical study investigates the effectiveness of ozone therapy in comparison to conventional treatment for alveolar osteitis (AO), a common painful complication following tooth extraction. Forty patients diagnosed with dry socket will be randomly divided into two groups. Group A will receive traditional treatment with normal saline irrigation and analgesics, while Group B will be treated using ozonated water, ozonated gel, and analgesics. Both groups will be monitored over a two-week period to evaluate pain levels, healing progression, and other clinical indicators. The study aims to assess the palliative and regenerative benefits of ozone therapy in managing AO, potentially offering an alternative to conventional symptomatic treatments.",[28],"2025-07-29",{"date":64,"type":37},"2025-08-06",{"date":66,"type":21},"2025-08-01",{"date":68,"type":21},"2026-02-01",{"name":70,"class":44},"Menoufia University",{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":17,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":4,"studyType":57,"phases":80,"briefSummary":82,"conditions":83,"keywords":84,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":98},"100579380","phase-2-a-comparative-single-blind-clinical-study-on-the-effect-of-alvogyl-eugenol-and-nigella-sativa-black-seed-oil-for-alveolar-osteitis-100579380","NCT06823544","A Comparative Single Blind Clinical Study on the Effect of Alvogyl, Eugenol, and Nigella Sativa (Black Seed Oil) for Alveolar Osteitis.","Inclusion Criteria:\n\n1. Patients over the age of 16, from both genders, who had their teeth extracted and were clinically diagnosed with dry socket.\n2. Absence of systematic disease.\n\nExclusion Criteria:\n\n1. SMOKER\n2. ALCOHOLIC\n3. Patients under the age of 16 years and over the age of 70 years\n4. Patient with various bone diseases including osteoporosis.\n5. Patients who had a history of taking oral or intravenous bisphosphonates.\n6. Patients with a history of radiotherapy to the head and neck and jawbones.","16 Years","70 Years",{"count":56,"type":21},[81],"PHASE2","Dry socket the unscientific term also known as alveolar or fibrinolytic osteitis is the most common postoperative complication following tooth extraction.\n\nTreatment of Alveolar osteitis can be either pharmacological on non-pharmacological. Management can be by irrigation, surgical intervention and placement of medicated dressing such as topical anti-bacterial, topical anesthetics and obtundants or combination of these three.this study aims to find the best and effective treatment for dry socket comparing Alveogyl, Eugenol and Black seed oil at this institution.",[28],[28,85,86,87,88],"Alvogyl","Black seed oil","Eugenol","Extraction socket","2025-02-07",{"date":91,"type":37},"2025-02-12",{"date":93,"type":21},"2025-02-01",{"date":95,"type":21},"2025-08-31",{"name":97,"class":44},"HITEC-Institute of Medical Sciences",1]