[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"bleeding-gum\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:bleeding-gum":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,84],{"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":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100558738","oral-health-intervention-in-adult-primary-care-100558738",false,"NCT06555029","Oral Health Intervention in Adult Primary Care","Multi-Level Interventions to Reduce Oral Health Disparities Among Adults in Primary Care Settings","Inclusion Criteria:\n\nPractices:\n\n* Use Epic EHR\n* Have older adults covered by Medicaid\n* Located within 60 miles of the CWRU research offices\n\nProvider (medical staff or clinician):\n\nMedical staff (MA, nurse):\n\n* Do not float between practices\n* Plan not to leave practice within a year\n* Provide a signed and dated consent form\n\nClinicians (Physician, NP):\n\n* Have a minimum of 2 patient-care days per week\n* Do not float between practices\n* Plan not to leave practice within a year\n* Provide signed and dated consent form\n\nOlder Adult\u002FPatient Participant:\n\n* Enrolled in CareSource Medicaid Plan\n* Female or male aged 55 years or older\n* Attending non-urgent primary care visits (PCV) at enrolled site\n* Provide signed and dated informed consent form\n* Planning to stay in the immediate area for the next year\n* Enrolled in the Adult Wellness Registry\n\nExclusion Criteria:\n\n* The presence of any serious medical health condition (such as dementia or other cognitive disorder not allowing them to participate) where the clinician indicates they should not participate.\n* The presence of any serious mental health disorders such as schizophrenia where the clinician indicates they should not participate.",true,"ALL","55 Years",{"count":20,"type":21},929,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study is a Stage III cRCT to test the efficacy of multi-level interventions at the practice- and provider-level to address low dental utilization (attendance) among Medicaid-enrolled older adults 55 years or older attending non-urgent primary care visits (PCV) in MetroHealth practice settings. Twelve practices will be randomized into two arms: A) Intervention arm will receive the multi-level intervention that includes: 1. Practice-level: EHR changes to include: ask, advise, assess, and connect (AAAC) strategies; 2. Provider-level: Medical staff (MA, nurse): Training in the AAAC process and complete AAAC for enrolled older adults; Clinicians (physician\u002Fnurse practitioner): CSM-based education (didactic), skills training (video training with standardized patients), and view completed AAAC in EHR to deliver core oral health (OH) facts to older adults, reinforce importance of dental visits, and document in EHR that OH facts were delivered. B) Control arm will receive, at the provider-level only (clinicians), non-theory-based information about retaining a healthy mouth using the ADA Mouth Healthy Series and deliver standard OH care for patients. Older Adults will be followed at 12 months and 24 months to determine if the participant had any dental attendance.\n\nThe primary objective is to test the efficacy of the practice level EHR strategy to ask \\[OH risk assessment\\], advise \\[going to dentist\\], assess \\[willingness for referral\\], and connect \\[eReferral, resources\\] together with clinician theory-based education to communicate OH facts versus clinician alone (standard oral health care) in increasing dental attendance in primary care settings.\n\nThe secondary objectives are to assess oral hygiene behavior, Geriatric Oral Health Quality of life, biometric measures (BP, serum cholesterol, blood glucose, hbA1c) abstracted from EHR data, potential mediators and moderators to investigate pathways that affect the primary and secondary outcomes, and assess implementation strategies: adoption, reach, fidelity, and maintenance of providers and practices that affect older adult primary and secondary outcomes.\n\nThe hypothesis is that medical staff completing the AAAC strategy and clinicians with improved OH knowledge (chronicity, systemic effects) will deliver consistent oral health messaging to older adults at PCVs that will result in increased preventive and restorative dental utilization compared to those providers delivering standard care.",[27,28,29,30],"Dental Caries","Dry Mouth","Periodontal Diseases","Bleeding Gum",[32,33,34,35,36],"Oral Health","Primary Care","Older Adults","Common Sense Model of Self-Regulation","EHR Modifications (Oral Health Questions and Referral)","RECRUITING","2025-10-13",{"date":40,"type":41},"2025-10-15","ACTUAL",{"date":43,"type":41},"2024-09-25",{"date":45,"type":21},"2028-10-30",{"name":47,"class":48},"Case Western Reserve University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":16,"sex":17,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":22,"phases":61,"briefSummary":63,"conditions":64,"keywords":69,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":49},"100583917","phase-3-efficacy-of-resveratrol-containing-mouthwash-in-reducing-halitosis-related-porphyrymonas-gingivalis-100583917","NCT06882564","Efficacy of Resveratrol Containing Mouthwash in Reducing Halitosis Related Porphyrymonas Gingivalis.","Efficacy of Resveratrol Containing Mouthwash in Reducing Halitosis Related Porphyromonas Gingivalis: A Randomized, Triple-blind Clinical Trial","Inclusion Criteria:\n\n* Organoleptic tongue of scores \\> 2 using (0-5scale) (Rosenberg and McCulloch, 1992)\n* Male and female undergraduate dental students without chemical plaque control measures for at least one weak\n* Male and female students with halitosis due to gingivitis\n* The age of students ranges from 20 to 23 years.\n* No periodontal treatment for at least one month\n* No systemic disease\n* No tobacco smoking\n* The patients must have at least 20 teeth\n\nExclusion Criteria:\n\n* Smokers and alcoholics\n* Patient with periodontitis or pocket depth \\> 6mm\n* Patient with orthodontics appliance\n* Open carious lesions, pericoronitis, dry socket, and fistula.\n* Patients with systemic disease and condition\n* taking medication in the last two weeks\n* Take garlic, onion, or licorice in the last 24 hours\n* using oral hygiene products in the last 24 hours\n* pregnant women\n* sinusitis, tonsilitis, and upper respiratory tract infection","20 Years","24 Years",{"count":60,"type":21},54,[62],"PHASE3","The aim of the study:\n\nTo assess the efficacy of antioxidant (resveratrol) mouthwash in reducing the level of p. gingivitis and oral malodor over 7 day period among undergraduate dental student patients from Mustansiriyah University\u002FCollege of Dentistry and Wasit University \u002FCollege of Dentistry.\n\nObjectives:\n\n* To assess the efficacy of anti-oxidant and anti-inflammatory resveratrol mouthwash in reducing halitosis in undergraduate students with plaque-induced gingivitis patients.\n* To assess the efficacy of resveratrol mouthwash in reducing p. gingivalis in undergraduate students' patients with oral malodor.\n* To determine the relation between p.gingivalis and clinical periodontal parameters (plaque index, gingival index, bleeding on probing) among undergraduate students with plaque-induced gingivitis and halitosis.",[65,66,67,30,68],"Halitosis","Mouth Disease","Plaque Induced Gingival Disease","Peridontal Disease",[70,71,72,73,74],"halitosis","plaque","gingivitis","resveratrol","chlorhexidine","2025-03-16",{"date":77,"type":41},"2025-03-18",{"date":79,"type":41},"2025-01-05",{"date":81,"type":21},"2025-11-01",{"name":83,"class":48},"Al-Mustansiriyah University",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":16,"sex":17,"minAge":91,"maxAge":92,"enrollmentInfo":93,"targetDuration":4,"studyType":22,"phases":95,"briefSummary":96,"conditions":97,"keywords":100,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":49},"100568729","evaluation-of-dental-and-periodontal-health-after-ipr-in-patients-in-orthodontic-treatment-with-clear-aligners-100568729","NCT06685016","Evaluation of Dental and Periodontal Health After IPR in Patients in Orthodontic Treatment With Clear Aligners","Evaluation of Dental and Periodontal Health After Interproximal Enamel Reduction, in Patients in Orthodontic Treatment With Clear Aligners, and Comparison Between Laser Diode and Sodium Fluoride for the Treatment of Dentin Hypersensitivity","Inclusion Criteria:\n\n* to be in orthodontic treatment with clear aligners and this treatment requires interproximal enamel reduction;\n* permanent dentition;\n* good oral and periodontal health.\n\nExclusion Criteria:\n\n* enamel defects;\n* cervical caries;\n* periodontal disease;\n* history of trauma or craniofacial anomalies;\n* pregnancy.","17 Years","100 Years",{"count":94,"type":21},30,[24],"This study aimed to evaluate dental and periodontal health after interproximal enamel reduction and to compare Laser diode (a device used in the Orthodontic Program) and sodium fluoride (often used in the Orthodontic Program and in the Material Dental Program). The hypothesis was that the intervention groups would show a lower dentin hypersensitivity incidence than the control group during orthodontic treatment.",[98,99,30],"Dentinal Hypersensitivity","Plaque, Dental",[101,102],"Clear Aligners","Interproximal enamel reduction","2024-11-12",{"date":105,"type":41},"2024-11-14",{"date":107,"type":41},"2023-06-24",{"date":109,"type":21},"2024-12",{"name":111,"class":48},"University of Campania Luigi Vanvitelli"]