[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"University of Bari Aldo Moro\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":252},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,44,74,102,128,150,174,202,229],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100631807","artificial-intelligence-based-assessment-of-endosseous-lesions-100631807",false,"NCT07505485","Artificial Intelligence-Based Assessment of Endosseous Lesions","Artificial Intelligence-Based Assessment of Endosseous Lesions: A Prospective Clinical Study","AIpreop","Inclusion Criteria:\n\n* Good health according to the System of the American Society of Anesthesiology\n* Aged older than 18 years\n* No general medical contraindication for surgery\n\nExclusion Criteria:\n\n* Smoking more than 15 cigarettes a day\n\n  * Pregnancy\n  * Acute infections",true,"ALL","18 Years","80 Years",{"count":22,"type":23},10,"ESTIMATED","INTERVENTIONAL",[26],"NA","Despite these advances, CBCT interpretation remains largely qualitative and dependent on the clinician's experience. Conventional evaluation is based on two-dimensional slices and linear measurements, which may underestimate lesion complexity and spatial distribution.\n\nRecent developments in Artificial Intelligence in Medicine have introduced automated image segmentation tools capable of identifying lesion boundaries and calculating volumetric data. These technologies allow a transition from subjective assessment to objective, reproducible quantification.\n\nThe potential clinical advantages include:\n\n* Objective measurement of lesion size (volume in mm³)\n* Improved surgical planning\n* Enhanced prediction of anatomical involvement\n* Reduction of diagnostic errors\n* Standardization of follow-up and outcome assessment Therefore, the aim of the present study was to evaluate the clinical impact of AI-based segmentation and volumetric analysis of endosseous lesions compared to conventional CBCT interpretation.",[29,30],"Maxillary Cyst","Mandibular Cyst","RECRUITING","2026-04-12",{"date":34,"type":35},"2026-04-15","ACTUAL",{"date":37,"type":23},"2026-04-01",{"date":39,"type":23},"2026-05-01",{"name":41,"class":42},"University of Bari Aldo Moro","OTHER",2,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":18,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":24,"phases":55,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100629988","impact-of-combined-cardio-pulmonary-assessment-on-copd-clinical-management-100629988","NCT07481825","Impact of Combined Cardio-pulmonary Assessment on COPD Clinical Management.","Impact of Combined cARdio-pUlmonary aSsessment on COPD Clinical Management: the ICARUS Study","ICARUS","Inclusion Criteria:\n\nPatients enrolled in the study should be diagnosed as COPD according to international recommendations (1) with the following features:\n\n* Post-bronchodilator FEV1 ≥ 50% or FEV1 z ≥ -2.5\n* Age \\> 40 years\n\nAdditionally, enrolled patients must fulfill at least one of the following cardiovascular criteria:\n\n* Very high cardiovascular risk\n\n  * according to SCORE2 (12)for patient \\\u003C 70 years old and defined as follows:\n\n    * Patients \\\u003C 50 years old \\> 7.5%\n    * Patients 50-69 years old \\> 10%\n  * according to SCORE OP 2 (13) calculator for patients \\> 70 years old and defined as \\> 15%\n* History of ischemic heart disease\n* Chronic or transient atrial fibrillation\n* Chronic heart failure with preserved (HFpEF) or mildly reduced (HFmrEF) ejection fraction (EF \\> 40%) (14)\n\nExclusion Criteria:\n\n* Post-bronchodilator FEV1 \\\u003C 50% or FEV1 z \\\u003C -2.5\n* LTOLT\n* Active neoplasm\n* Patient unable to perform lung function\n* Pregnancy","41 Years",{"count":54,"type":23},350,[26],"The goal of this randomized clinical trial is to learn whether a combined cardio-pulmonary assessment improves cardiac function, exercise capacity, cardiac biomarkers and health-related quality of life in adults with mild-to-moderate chronic obstructive pulmonary disease (COPD) who are at high cardiovascular risk or have established cardiovascular disease.\n\nThe main questions it aims to answer are:\n\n* Does the combined cardio-pulmonary assessment improve mean left ventricular ejection fraction (EF) over 12 months compared with standard respiratory care?\n* Does the combined cardio-pulmonary assessment improve mean 6-minute walk distance (6MWD) over 12 months compared with standard respiratory care?\n* Does the combined cardio-pulmonary assessment reduce mean NT-proBNP over 12 months compared with standard respiratory care?\n* Does the combined cardio-pulmonary assessment improve mean Kansas City Cardiomyopathy Questionnaire (KCCQ-12) score over 12 months compared with standard respiratory care?\n\nResearchers will compare a combined cardio-pulmonary assessment to standard respiratory care to see whether the integrated approach leads to greater improvements in EF, 6MWD, NT-proBNP, and KCCQ-12.\n\nParticipants will:\n\n* Be randomly assigned to receive either a combined cardio-pulmonary assessment or standard respiratory care\n* Complete a baseline visit that includes clinical assessment, respiratory function testing, blood tests (including NT-proBNP), a 6-minute walk test, and the KCCQ-12 questionnaire\n* Undergo cardiovascular evaluation (electrocardiogram and transthoracic echocardiography) if assigned to the combined assessment group\n* Attend follow-up evaluation at 12 months, repeating the same assessments according to their assigned group",[58,59],"COPD (Chronic Obstructive Pulmonary Disease)","Cardiovascular Disease",[61,62,63,64],"COPD","Chronic Obstructive Pulmonary Disease","Cardiovascular","cardio-pulmonary","NOT_YET_RECRUITING","2026-03-15",{"date":68,"type":35},"2026-03-19",{"date":70,"type":23},"2026-09",{"date":72,"type":23},"2029-11",{"name":41,"class":42},{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":79,"acronym":80,"eligibilityCriteria":81,"healthyVolunteers":17,"sex":18,"minAge":82,"maxAge":20,"enrollmentInfo":83,"targetDuration":4,"studyType":24,"phases":85,"briefSummary":86,"conditions":87,"keywords":90,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":101,"locationsCount":4},"100621477","therapeutic-wavelength-nanotechnology-devices-in-alveolar-preservation-100621477","NCT07371130","Therapeutic Wavelength Nanotechnology Devices in Alveolar Preservation","Evaluation of Low-Intensity Therapeutic Wavelength Nanotechnology Devices in Alveolar Preservation: A Clinical Trial","APnanotecnolog","Inclusion Criteria:\n\n* Adults in good general health\n* Indication for tooth extraction in sites planned for delayed implant placement\n* Inability to place immediate post-extraction implants due to insufficient residual bone to ensure primary stability\n* Extraction sockets presenting absence of the buccal (vestibular) bone wall\n* Signed informed consent\n\nExclusion Criteria:\n\n* Systemic conditions affecting bone healing\n* Uncontrolled periodontal disease\n* Smoking \\>10 cigarettes\u002Fday\n* Pregnancy or lactation\n* Use of medications interfering with bone metabolism","21 Years",{"count":84,"type":23},20,[26],"After tooth extraction, a progressive alveolar bone resorption is observed. Alveolar ridge preservation consists of placing a biomaterial within the extraction socket and covering it with a membrane.\n\nThis procedure helps limit physiological bone resorption, making the soft and hard tissue profile of the edentulous site more prosthetically favorable.",[88,89],"Tooth Avulsion","Tooth Crown Fracture",[91,92,93,94],"alveolar ridge preservation","alveolar preservation","bone loss","bone preservation","2026-02-04",{"date":97,"type":35},"2026-02-05",{"date":99,"type":23},"2026-02-15",{"date":39,"type":23},{"name":41,"class":42},{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":108,"eligibilityCriteria":109,"healthyVolunteers":17,"sex":18,"minAge":110,"maxAge":20,"enrollmentInfo":111,"targetDuration":4,"studyType":24,"phases":113,"briefSummary":114,"conditions":115,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":119,"lastUpdatePostDateStruct":120,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":127},"100623235","autogenous-tooth-transplantation-with-instrumentally-simulated-open-apex-and-platelet-rich-fibrin-100623235","NCT07393997","Autogenous Tooth Transplantation With Instrumentally Simulated Open Apex and Platelet-Rich Fibrin","Clinical Evaluation of Autogenous Tooth Transplantation With Instrumentally Simulated Open Apex and Autologous Platelet-Rich Fibrin (PRF) Support in Teeth With Complete Root Formation","OpenApexT","Inclusion Criteria:\n\nAutotransplantation will be performed in selected cases with favorable biological and functional prognosis, including:\n\n* Early loss of permanent teeth due to trauma, extensive caries, or agenesis.\n* Dental agenesis, particularly involving premolars or incisors, when a suitable donor tooth is available.\n* Replacement of non-restorable teeth (fractures or destructive caries).\n* Preservation of alveolar bone in growing patients where implant therapy is contraindicated.\n* Functional and aesthetic rehabilitation of anterior teeth in pediatric and adolescent patients.\n* Post-traumatic oral rehabilitation in young patients.\n* Good general and oral health.\n* Presence of a vital and intact periodontal ligament on the donor tooth.\n* Adequate recipient site dimensions and morphology, or surgically adaptable.\n* Absence of active infection at the recipient site. Donor Tooth Selection Criteria\n* Tooth extracted for orthodontic purposes.\n* Impacted or erupting third molars with compatible morphology.\n* Suitable supernumerary teeth.\n\nExclusion Criteria:\n\n* Poor patient compliance.\n* Active infection at the recipient site.\n* Smoking of more than 15 cigarettes a day\n\n  •. Untreated periodontal disease\n* Pregnancy or breastfeeding at date of inclusion\n* Acute infections","10 Years",{"count":112,"type":23},5,[26],"Autogenous tooth transplantation (autotransplantation) represents a biologically valid alternative to implant therapy, particularly in young patients where implant placement is contraindicated due to ongoing skeletal growth. This approach preserves alveolar bone volume, maintains periodontal proprioception, and allows physiological adaptation over time.",[116,117,118],"Tooth Loss","Tooth Diseases","Reimplant; Complications","2026-01-30",{"date":121,"type":35},"2026-02-06",{"date":123,"type":35},"2026-01-01",{"date":125,"type":23},"2026-09-01",{"name":41,"class":42},1,{"id":129,"slug":130,"hasResults":11,"nctId":131,"briefTitle":132,"officialTitle":133,"acronym":4,"eligibilityCriteria":134,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":135,"enrollmentInfo":136,"targetDuration":4,"studyType":24,"phases":137,"briefSummary":138,"conditions":139,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":127},"100606589","primary-stability-and-peri-implant-outcomes-of-short-implants-in-post-extraction-single-tooth-sites-100606589","NCT07177521","Primary Stability and Peri-implant Outcomes of Short Implants in Post-extraction Single-tooth Sites","Primary Stability and Peri-implant Outcomes of Short Implants in Post-extraction Single-tooth Sites: a Randomized Controlled Trial.","Inclusion Criteria:\n\n* Age ≥18 years.\n* Single-tooth post-extraction sites requiring immediate implant placement in posterior regions (premolars\u002Fmolars) or selected anterior sites.\n* Planned short implant (≤7-8 mm length, 3.5-5.0 mm diameter).\n* Adequate oral hygiene, no active periodontal disease.\n* Written informed consent.\n\nExclusion Criteria:\n\n* Heavy smoking (\\>20 cigarettes\u002Fday).\n\n  * Uncontrolled diabetes or systemic conditions affecting bone healing.\n  * Current bisphosphonate\u002Fantiresorptive therapy.\n  * Immunosuppression, pregnancy.\n  * Poor oral hygiene or acute infection at site.\n  * Severe bone dehiscence preventing primary stability.","75 Years",{"count":22,"type":23},[26],"The placement of short implants in post-extraction sockets is a valuable option when residual bone height is limited, minimizing morbidity and treatment time. The management of the peri-implant gap and soft tissues may influence primary stability, hard\u002Fsoft tissue remodeling, and implant success.",[140,116,141],"Edentulous Jaw","Toothless Mouth","2026-01-23",{"date":144,"type":35},"2026-01-27",{"date":146,"type":35},"2025-01-10",{"date":148,"type":23},"2026-08-10",{"name":41,"class":42},{"id":151,"slug":152,"hasResults":11,"nctId":153,"briefTitle":154,"officialTitle":155,"acronym":156,"eligibilityCriteria":157,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":135,"enrollmentInfo":158,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":161,"conditions":162,"keywords":4,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":173,"locationsCount":4},"100608246","occlusal-load-distribution-and-periodontal-status-100608246","NCT07199062","Occlusal Load Distribution and Periodontal Status","Correlation Between Occlusal Load Distribution and Periodontal Status: A Cohort Study","Perio-Occlusio","Inclusion Criteria:\n\n* Adults (≥18 years).\n* Presence of natural dentition, fixed prostheses, or implant-supported fixed prostheses.\n* Ability to undergo radiological (OPT) and periodontal examinations.\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Patients wearing removable prostheses.\n* Severe systemic conditions contraindicating dental treatment.\n* Inability to provide informed consent.",{"count":159,"type":23},50,"OBSERVATIONAL","Occlusal forces are unevenly distributed among teeth during mastication, potentially predisposing certain teeth to higher functional loads. Teeth subjected to increased occlusal loading may be at greater risk of periodontal breakdown, especially in patients with pre-existing periodontal disease.\n\nTechnological advances, such as mandibular movement recording systems, allow for precise assessment of occlusal contacts and load distribution. However, the relationship between occlusal loading patterns and periodontal status remains insufficiently investigated.\n\nThis study aims to evaluate whether teeth exposed to higher masticatory loads show an association with periodontal disease severity.",[163,164,165,166],"Periodontal Diseases","Periodontal Pocket","Periodontitis","Periimplantitis","2025-09-21",{"date":169,"type":35},"2025-09-30",{"date":171,"type":23},"2025-10-01",{"date":37,"type":23},{"name":41,"class":42},{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":180,"eligibilityCriteria":181,"healthyVolunteers":17,"sex":18,"minAge":4,"maxAge":4,"enrollmentInfo":182,"targetDuration":184,"studyType":160,"phases":4,"briefSummary":185,"conditions":186,"keywords":190,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":194,"lastUpdatePostDateStruct":195,"startDateStruct":197,"completionDateStruct":199,"leadSponsor":201,"locationsCount":4},"100603269","from-conflict-to-family-trauma-100603269","NCT07134322","From Conflict to Family Trauma","From Conflict to Family Trauma - A Longitudinal Research for the Development of Best Practices in the Italian Legal System","FamilyTrauma","Inclusion Criteria:\n\n* Families with minor children who file a lawsuit\n* Parent-child relationships must have been severed with at least one parent.\n\nExclusion Criteria:\n\n\\- Families with adult children",{"count":183,"type":23},200,"12 Months","This project will examine the experience of the researcher as expert in the family court dealing with questions regarding family units, in conflict and children, victims of the family conflict, victims of abuse and neglect, often repeated over time.After the first consultation, family conflict often recurs, without regard for the treatment received, returning to the civil courts and sometimes to the criminal courts. There are three possibilities at this point, following the first decision of the court (a) there is a separation that resolves conflicts and leads to an improvement in outcomes for the children concerned; (b) pre-existing conditions specific to the children concerned continue, and the decision of the court regading separation has no effect; (c) conflict between the parents continues, with repeated returns to the civil courts, failure of processes of mediation and negotiation, and continuing or exacerbated trauma to the child leading to worse outcomes; (d) where there is a worse outcome, this may be due to the lack of supports following the expert psychological assessment and recommendation to the court..The forensic evaluation of the family often refers the family to public health services for therapeutic interventions and social supports. The lack of these interventions and supports of public health services may exacerbate the family trauma. This may occur (a) because the family conflict continues in the absence of the interventions and supports; (b) because the family trauma is exacerbated by continuing court proceedings because the conflict between parents concerning the care and placement of the children leads to prolonged legal proceedings and may result in worse outcomes for the children, such as criminal behaviour as this struggle continues. The child is 'instrumentalised', used as a pawn or weapon in the struggle between the parents. The research project aims first of all to outline, on the basis of the data to be acquired, (a) whether there is evidence that the decision of the court guided by the expert opinion and recommendations has a beneficial effect on outcomes for the child; (b) specific lines of treatment intervention and better packages of care and support to enhance good outcomes and minimise or prevent these adverse outcomes, under the supervision of the judge.",[187,188,189],"Family Conflict","Family Characteristics","Family Dysfunctional",[191,192,193],"Family Trauma","Higth Conflict","Therapeutic Jurisprudence","2025-08-20",{"date":196,"type":35},"2025-08-21",{"date":198,"type":23},"2026-02-08",{"date":200,"type":23},"2026-12-20",{"name":41,"class":42},{"id":203,"slug":204,"hasResults":11,"nctId":205,"briefTitle":206,"officialTitle":207,"acronym":208,"eligibilityCriteria":209,"healthyVolunteers":11,"sex":18,"minAge":19,"maxAge":4,"enrollmentInfo":210,"targetDuration":4,"studyType":24,"phases":212,"briefSummary":213,"conditions":214,"keywords":216,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":221,"lastUpdatePostDateStruct":222,"startDateStruct":224,"completionDateStruct":226,"leadSponsor":228,"locationsCount":127},"100534397","rapid-de-escalation-of-anti-mrsa-therapy-guided-by-s-aureus-nares-screening-in-case-of-pneumonia-100534397","NCT06238297","Rapid De-escalation of Anti-MRSA Therapy Guided by S. Aureus Nares Screening in Case of Pneumonia","Rapid De-escalation of Anti-MRSA Therapy Guided by S. Aureus Nares Screening in Case of Pneumonia (SNAP Study)","SNAP","Inclusion Criteria:\n\n* Subjects 18 years or older.\n* Patients hospitalized at the Azienda Consorziale Policlinico di Bari;\n* Clinical diagnosis of CAP\u002FHAP\u002FVAP;\n* Commitment by the prescribing physician to set an anti-MRSA antibiotic therapy in empirical\n* Enrollement within 48h from the beginning of the empirical anti-MRSA therapy.\n\nExclusion Criteria:\n\n* Febrile neutropenia or severe immunodeficiency;\n* Chronic airway infection (eg cystic fibrosis);\n* Suspect of extrapulmonary infection by MRSA\n* Refusal by the patient or legal guardian;\n* Refusal by the physician in charge of the patient to perform antibiotic de-escalation based on the result of the nasal swab;\n* Enrollment after 48 hours from the beginning of the empirical anti-MRSA therapy.",{"count":211,"type":23},76,[26],"The current IDSA\u002FATS guidelines recommend Linezolid and Vancomycin for MRSA coverage in hospitalized patients with pneumonia, which is common clinical practice in Italy. However, a nasal PCR-assay for MRSA has a high negative predictive value and can facilitate rapid antibiotic de-escalation, thereby avoiding unnecessary anti-MRSA treatments. The indiscriminate use of these drugs has contributed to the emergence of resistant S. aureus strains and has led to significant adverse effects, without providing any survival benefits. Additionally, it has increased hospital stays and associated costs. The proposed study aims to use this diagnostic tool to shorten empirical anti-MRSA treatment duration in pneumonia patients, focusing on reducing antimicrobial therapy days while measuring in-hospital mortality, length of stay and adverse drug event incidence.",[215],"Pneumonia, Bacterial",[217,218,219,220],"MRSA","Antimicrobial stewardship","Randomized trial","Pneumonia","2025-05-23",{"date":223,"type":35},"2025-05-30",{"date":225,"type":35},"2024-05-06",{"date":227,"type":23},"2025-06-30",{"name":41,"class":42},{"id":230,"slug":231,"hasResults":11,"nctId":232,"briefTitle":233,"officialTitle":234,"acronym":235,"eligibilityCriteria":236,"healthyVolunteers":17,"sex":18,"minAge":237,"maxAge":238,"enrollmentInfo":239,"targetDuration":4,"studyType":160,"phases":4,"briefSummary":241,"conditions":242,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":244,"lastUpdatePostDateStruct":245,"startDateStruct":247,"completionDateStruct":249,"leadSponsor":251,"locationsCount":127},"100553667","study-of-the-thyroid-function-and-echostructural-morphology-in-patients-affected-with-rasopathies-ecoras2023-100553667","NCT06489067","Study of the Thyroid Function and Echostructural Morphology in Patients Affected With Rasopathies (ECORAS2023)","Study of the Thyroid Function and Echostructural Morphology in Patients Affected With Rasopathies. An Italian Multicenter Study","ECORAS2023","Inclusion Criteria:\n\n* Genetically confirmed RASopathy\n* Age 3-25 years\n\nExclusion Criteria:\n\n* Previous radiotherapy treatments, known exposure to ionizing radiation\n* Iodine deficiency\n* Use of iodine-based compounds or drugs that interfere with thyroid function\n* Congenital hypothyroidism\u002Fhyperthyroidism\n* Severe obesity with metabolic complications","3 Years","25 Years",{"count":240,"type":23},115,"The study aims to evaluate the prevalence of thyroid disease, particularly with autoimmune pathogenesis (isolated hyperthyrotropinemia, hyperthyroidism, hypothyroidism, thyroid nodules) and\u002For morphostructural abnormalities of the thyroid gland in patients with RASopathy genetically confirmed by NGS technique (analysis of the genes: BRAF, CBL, HRAS, KRAS, LZTR1, MAP2K1, MAP2K2, MRAS, NRAS, PPP1CB, PTPN11, RAF1, RIT1, RRAS2, SHOC2, SOS1, SOS2) and to compare the data obtained in our sample with those of the general population.\n\nThe secondary aim of the study is to evaluate the association between vitamin D deficiency and\u002For other abnormalities of bone metabolism and thyroid disease and\u002For morphostructural anomalies of the thyroid gland in patients with RASopathy.",[243],"RASopathy","2024-07-03",{"date":246,"type":35},"2024-07-05",{"date":248,"type":35},"2024-01-15",{"date":250,"type":23},"2024-06-30",{"name":41,"class":42},""]