[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Juan Gonzalo Olivieri\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":72},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"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":30,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100403424","carious-tissue-selective-removal-on-permanent-posterior-teeth-100403424",false,"NCT04533113","Carious Tissue Selective Removal on Permanent Posterior Teeth.","Carious Tissue Selective Removal on Permanent Posterior Teeth. A Randomized Controlled Clinical Study.","Inclusion Criteria:\n\n* Patients that demonstrate understanding of the study and willingness to participate as evidenced by signing the voluntary informed consent and received a signed and dated copy of the informed consent form.\n* Understands and is willing to comply with all study procedures and restrictions.\n* Not presence of clinically significant and relevant abnormalities of clinical history or oral examination.\n* Diagnosis of normal pulp or reversible pulpitis.\n* No presence of periapical periodontitis\n* Posterior teeth\n\nExclusion Criteria:\n\nGeneral: Patients with systemic diseases, diabetes, immunocompromised and pregnant women, or any clinically significant or relevant oral abnormalities.\n\nSpecific: Impossibility of restoration, diagnosis of irreversible pulpitis or necrosis, preoperative pain",true,"ALL","18 Years","75 Years",{"count":21,"type":22},111,"ESTIMATED","INTERVENTIONAL",[25],"NA","This study is a prospective randomized controlled study of patients who come to the University. The aim is to evaluate the success rate of selective removal of carious tissue in deep lesions of posterior teeth. Three different materials will be used as liners (VitreBond ™Plus, BioDentine™, and Theracal™ LC). Post-operative pain, clinical, and radiographic success will be evaluated at one, two, and five-year follow-up. The null hypothesis is that there will be no statistically significant differences in rates of successful treatment with the three materials used.",[28,29],"Dental Caries","Dental Materials",[31,32,33,34],"Dental caries","Dental materials","Outcome","Postoperative Pain","RECRUITING","2020-08-27",{"date":38,"type":39},"2020-08-31","ACTUAL",{"date":41,"type":39},"2019-02-20",{"date":43,"type":22},"2026-07",{"name":45,"class":46},"Juan Gonzalo Olivieri","OTHER",1,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":4,"eligibilityCriteria":54,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":55,"targetDuration":4,"studyType":23,"phases":57,"briefSummary":58,"conditions":59,"keywords":62,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":66,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":47},"100403106","outcome-of-endodontic-treatment-and-retreatment-with-a-bioceramic-sealer-100403106","NCT04528979","Outcome of Endodontic Treatment and Retreatment With a Bioceramic Sealer","The Outcome of Endodontic Treatment and Retreatment With a Bioceramic Sealer: A Prospective Randomized Controlled Clinical Study","Inclusion Criteria:\n\n* Patients that demonstrate understanding of the study and willingness to participate as evidenced by signing the voluntary informed consent and received a signed and dated copy of the informed consent form.\n* Understands and is willing to comply with all study procedures and restrictions.\n* Not presence of clinically significant and relevant abnormalities of clinical history or oral examination.\n* Diagnosis of irreversible pulpitis or apical symptomatic \u002F asymptomatic periodontitis.\n* Retreatment cases due to an endodontic failure.\n* Single or bi-radicular teeth.\n\nExclusion Criteria:\n\n* General: Patients with systemic diseases, diabetes, immunocompromised and pregnant women, or any clinically significant or relevant oral abnormalities.\n* Specific: root resorption, root fractures, impossibility of restoration and cases were primary or secondary root canal treatment is not the treatment of choice.",{"count":56,"type":22},220,[25],"This study is a prospective randomized controlled study of patients who come to the University. The aim is to evaluate the success rate of treatment and retreatment of canals using BioRoot ™ RCS cement compared with AH Plus up to 6 years of follow-up. The null hypothesis is that there will be no statistically significant differences in rates of successful treatment of root canals filled with BioRoot ™ RCS compared to gutta-percha and AH Plus sealer.",[60,61],"Endodontic Disease","Endodontically Treated Teeth",[63,64,33,65],"Primary root canal treatment","Secondary root canal treatment","Root canal sealer",{"date":38,"type":39},{"date":68,"type":39},"2019-09-20",{"date":70,"type":22},"2027-01",{"name":45,"class":46},""]