[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"oral-health-related-quality-of-life\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:oral-health-related-quality-of-life":169},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,53,80,119,142],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":32,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":4},"100636711","patient-reported-outcomes-of-four-intraoral-suture-materials-100636711",false,"NCT07569237","Patient-Reported Outcomes of Four Intraoral Suture Materials","Patient-Reported Outcomes Following Application of Intraoral Sutures: A Split-Mouth Randomized Controlled Trial","Inclusion Criteria:\n\nAdults aged 20-30 years.\n\nSystemically healthy (ASA I-II).\n\nNo history of allergy to study suture materials.\n\nPeriodontally healthy, with no active oral lesions, including carious lesions.\n\nDental Requirements: All maxillary canine, second premolar, and first molar teeth present.\n\nMinimal (≤0.5 mm) open contacts between the pairs of teeth that define the study sites.\n\nIdeally, full maxillary dentition present from first molar to first molar.\n\nAt least 2 mm of keratinized tissue width on buccal intervention sites.\n\nWilling and able to provide informed consent.\n\nWilling and able to attend all study follow-up visits and complete study questionnaires.\n\nExclusion Criteria:\n\nAllergy to any study materials (e.g., suture materials or anesthetics) or medications (Paracetamol).\n\nAny systemic disease affecting wound healing (e.g., diabetes, immunosuppression).\n\nUse of any medications.\n\nPregnancy or lactation.\n\nUnwillingness or inability to provide informed consent.\n\nUnwillingness or inability to comply with study protocol and follow-up visits.\n\nExit Criteria:\n\nParticipants may exit the study at any time if they wish to discontinue participation.\n\nNoncompliance with study protocol and visits.\n\nDevelopment of conditions (e.g., infection) that require immediate care or that introduce exclusion criteria.",true,"ALL","20 Years","30 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","When patients undergo minor oral surgery, dentists use various types of stitches (sutures) to help the gums heal. These stitches can be made of different materials, and some might feel more comfortable, cause less pain, or interfere less with eating and speaking than others.\n\nThe purpose of this study is to compare four commonly used dental suture materials to see which ones patients prefer. Participants in this study will receive four different types of stitches in different areas of their upper jaw after a routine dental procedure.\n\nPatients will be asked to report their levels of pain, discomfort, and any difficulties with daily activities like eating and talking on Days 3, 7, and 14 after the procedure. A panel of dental specialists will also examine photos of the healing process to see if one material helps the mouth heal better than others. This research will help dentists choose the best materials to improve patient comfort after oral surgery.",[28,29,30,31],"Suture Materials","Wound Healing","Patient Comfort","Oral Health-Related Quality of Life",[33,34,35,36,37,38,39,40],"Split-mouth design","Patient-reported outcome measures (PROMs)","Intraoral sutures","Dental surgery","Visual Analog Scale (VAS)","Periodontology","Oral surgery healing","Braided vs Monofilament sutures","NOT_YET_RECRUITING","2026-04-28",{"date":44,"type":45},"2026-05-06","ACTUAL",{"date":47,"type":22},"2026-07",{"date":49,"type":22},"2028-04",{"name":51,"class":52},"University of Jordan","OTHER",{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":16,"sex":17,"minAge":61,"maxAge":4,"enrollmentInfo":62,"targetDuration":4,"studyType":64,"phases":4,"briefSummary":65,"conditions":66,"keywords":4,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":75,"leadSponsor":77,"locationsCount":79},"100617892","oral-health-in-palliative-care-a-survey-study-100617892","NCT07324525","Oral Health in Palliative Care: A Survey Study","Oral Health and Dental Care in Palliative Medicine: A Survey Study Among Patients and Members of the German Society for Palliative Medicine","OH-PAL","Inclusion Criteria:\n\n* consent-capable patients receiving palliative care\n* patients whose health status allows completion of a questionnaire\n* consent-capable members of the German Society for Palliative Medicine\n\nExclusion Criteria:\n\n* Participants under 18 years of age\n* Individuals who are unable or unwilling to provide informed consent","18 Years",{"count":63,"type":22},151,"OBSERVATIONAL","Oral health problems such as xerostomia or oral infections are common in palliative care patients and can significantly impair quality of life. Adequate dental care may contribute substantially to symptom control and well-being; however, oral health and dental services are often insufficiently integrated into palliative care practice. In addition, little is known about the level of awareness, knowledge, and interprofessional collaboration regarding oral health among palliative care professionals.\n\nThis prospective, non-interventional survey study aims to assess the relevance of oral health in palliative care by surveying both palliative care patients and healthcare professionals who are members of the German Society for Palliative Medicine. The study investigates patients' oral health status, oral health-related quality of life, and access to dental care, as well as professionals' knowledge, attitudes, and current practices related to oral health and dental care in palliative settings. The findings are intended to identify existing gaps and inform strategies for improved integration of dental expertise into palliative care.",[67,31,68,69],"Oral Health Care","Palliative Care","Palliative Care, Patient Care","RECRUITING","2026-02-24",{"date":73,"type":45},"2026-02-27",{"date":71,"type":45},{"date":76,"type":22},"2026-06",{"name":78,"class":52},"University Medical Center Goettingen",1,{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":4,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":87,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":23,"phases":90,"briefSummary":91,"conditions":92,"keywords":100,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":79},"100615440","the-effectiveness-of-the-twin-block-and-carriere-motion-appliances-in-post-pubertal-patients-and-an-evaluation-of-the-impact-of-class-ii-malocclusion-and-its-correction-on-oral-health-related-quality-of-life-100615440","NCT07292636","The Effectiveness of the Twin Block and Carriere Motion Appliances in Post-pubertal Patients and an Evaluation of the Impact of Class II Malocclusion and Its Correction on Oral Health-related Quality of Life","The Effectiveness of the Twin Block and Carriere Motion Appliances in Post-pubertal Patients and an Evaluation of the Impact of Class II Malocclusion and Its Correction on Oral Health-related Quality of Life: A Randomised Controlled Trial","Inclusion Criteria:\n\n1. males and females aged 14 ½ -16 years from the HSE waiting list,\n2. Cervical Vertebral Maturation (CVM) stage ≥5,\n3. a mild-moderate skeletal II pattern,\n4. normodivergent with average maxillomandibular planes angle (MMPA: 27±4 degrees),\n5. Class II division 1 incisor relationship,\n6. Class II molar relationship of ≥1\u002F2 unit bilaterally,\n7. overjet of ≥7 mm,\n8. ≤5mm of dental crowding in both arches and\n9. fluent English speaker.\n\nExclusion Criteria:\n\n1. high MMPA,\n2. low MMPA,\n3. have\u002Fhad cleft lip or palate or craniofacial syndrome,\n4. hypodontia,\n5. gross mandibular asymmetry,\n6. a medically diagnosed growth excess or deficiency,\n7. not dentally fit or\n8. had previously received orthodontic treatment.","14 Years",{"count":89,"type":22},88,[25],"The investigators of this clinical trial aim to:\n\n* Compare the effectiveness and efficiency of Clark's Twin Block Appliance (CTB) vs Carriere Motion Appliance (CMA) in correcting Class II malocclusion when used in post-pubertal older adolescents, in terms of skeletal and dental change.\n* Evaluate potential negative oral health-related quality of life (OHRQoL) impacts during the active treatment phase with either CTB or CMA in post-pubertal adolescents.\n* Investigate the impact of Class II malocclusion on oral health-related quality of life (OHRQoL) in post-pubertal adolescents.\n\nClass II division 1 malocclusion is a dental condition where the upper teeth protrude significantly over the lower teeth. It is a common type of malocclusion observed in orthodontic practice, accounting for approximately 20-25% globally. Correcting Class II malocclusion in growing patients using functional appliances and Class II correctors is relatively predictable.\n\nIn Ireland and the United Kingdom, the Clark's Twin Block (CTB) is the most commonly used functional appliance. The CTB consists of two components: one for the upper teeth and one for the lower teeth. These components are engineered to position the lower jaw forward, thereby promoting the desired dentoskeletal changes (moving the upper teeth back and lower forward). Another device used for Class II correction is the Carriere Motion Appliance (CMA). The CMA is gaining popularity as a treatment option for Class II malocclusion, inducing dental changes similar to those achieved with a CTB. However, uncertainty persists regarding the effectiveness of these appliances in older adolescents in the post-pubertal growth phase (aged approximately 14.5 years or above).\n\nAdditionally, although both CTB and CMA are effective in growing patients in correcting dental and skeletal discrepancies, they may influence daily activities, comfort, and psychological aspects, which often results in poor compliance. Poor adherence to orthodontic treatment, whether with fixed or removable appliances, can lead to higher rates of treatment failure.",[93,94,95,96,97,98,99,31],"CLASS II DIVISION 1 MALOCCLUSION","Class II Malocclusion","Growth","Overjet","Class II Buccal Segment Relationship","Class II Growth Modification","Distalization",[94,96,101,102,103,104,105,106,107,108,109],"Class II Molar Relationship","Class II Canine Relationship","Functional Appliance","Class II Corrector","Growth Modification","Oral Health Related Quality of Life","Twin Block","Carriere Motion Appliance","RCT","2025-12-15",{"date":112,"type":45},"2025-12-18",{"date":114,"type":22},"2026-03",{"date":116,"type":22},"2029-09",{"name":118,"class":52},"Aslam Alkadhimi",{"id":120,"slug":121,"hasResults":11,"nctId":122,"briefTitle":123,"officialTitle":124,"acronym":4,"eligibilityCriteria":125,"healthyVolunteers":11,"sex":17,"minAge":126,"maxAge":127,"enrollmentInfo":128,"targetDuration":4,"studyType":23,"phases":130,"briefSummary":131,"conditions":132,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":133,"lastUpdatePostDateStruct":134,"startDateStruct":136,"completionDateStruct":138,"leadSponsor":140,"locationsCount":4},"100571551","effect-of-oral-health-educational-program-on-oral-health-quality-of-life-of-group-of-type1-diabetes-children-100571551","NCT06721728","Effect of Oral Health Educational Program on Oral Health Quality of Life of Group of Type1 Diabetes Children","Effect of Oral Health Educational Program on the Oral Health-Related Quality of Life of a Group of Children With Type-1 Diabetes Mellitus: A Before and After Pilot Study","Inclusion Criteria:\n\n* Children of both sexes\n* Age from 8 to 10 years old\n* Diagnosed with type 1 diabetes mellitus\n\nExclusion Criteria:\n\n* Children with other systemic diseases\n* Parents who refuse participation","8 Years","10 Years",{"count":129,"type":22},50,[25],"The study is a before and after study made to assess the oral health related quality of life after oral health educational program on children with type1 diabetes mellitus.\n\nThe main questions it aims to answer are:\n\n* oral health related quality of life\n* caries experience\n\nParticipants will answer oral health quality of life questionnaire and will be checked for DMF and def indices and then given an oral health education program and followed up after 3 months.",[106],"2024-12-03",{"date":135,"type":45},"2024-12-06",{"date":137,"type":22},"2025-01-01",{"date":139,"type":22},"2025-07-01",{"name":141,"class":52},"Cairo University",{"id":143,"slug":144,"hasResults":11,"nctId":145,"briefTitle":146,"officialTitle":147,"acronym":4,"eligibilityCriteria":148,"healthyVolunteers":11,"sex":17,"minAge":61,"maxAge":149,"enrollmentInfo":150,"targetDuration":4,"studyType":23,"phases":152,"briefSummary":153,"conditions":154,"keywords":155,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":79},"100493333","oral-health-in-patients-with-severe-eating-disorders-100493333","NCT05703789","Oral Health in Patients With Severe Eating Disorders","Oral Health in Patients With Severe Eating Disorders An Interview, Questionnaire and Intervention Study With a Focus on Quality of Life","Inclusion Criteria:\n\n* Patients diagnosed with anorexia nervosa, bulimia nervosa or non-specific binge eating disorder for a minimum of 10 years = definition of a \"severe\" eating disorder where extensive dental damage can be anticipated to find.\n* Need of dental treatment of at least six teeth in one jaw,\n\nExclusion Criteria:\n\n* Age \\\u003C18 years or patients unable to provide informed consent.","50 Years",{"count":151,"type":22},90,[25],"The overall aim of the research project is to assess whether the quality of life of patients with severe eating disorders is improved by dental treatment.\n\nPatients diagnosed with anorexia nervosa, bulimia nervosa or non-specific binge eating disorder with extensive dental treatment need will be treated with resin composite restorations or prosthetic therapy. The primary outcome measures is oral health related quality of life. Secondary are orofacial functions and oral esthetics. Patients will be compared to a waiting list.",[106],[156,157,158,159],"prosthetic rehabilitation","eating disorder","quality of life","dental","2023-01-26",{"date":162,"type":45},"2023-01-30",{"date":164,"type":45},"2022-12-27",{"date":166,"type":22},"2027-11-15",{"name":168,"class":52},"Karolinska Institutet","Oral Health-related Quality of Life"]