[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100621819":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":30,"centralContacts":39,"locations":49,"responsibleParty":66,"collaborators":30,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":30,"eligibilityCriteria":76,"healthyVolunteers":77,"sex":78,"minAge":79,"maxAge":80,"enrollmentInfo":81,"targetDuration":30,"studyType":84,"phases":85,"briefSummary":87,"conditions":88,"keywords":92,"overallStatus":52,"whyStopped":30,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":111},{"fullName":5,"class":6},"Mustafa Kemal University","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Total Pulpotomy","EXPERIMENTAL","After the access cavity is prepared, the vitality of the pulp will be visually confirmed.\n\nThe coronal pulp tissue will be removed using a high-speed sterile diamond bur with copious water cooling.\n\nA cotton pellet moistened with 2.5% NaOCl will be applied to the pulp chamber. If necessary, this procedure will be repeated for up to 10 minutes. The time required to achieve hemostasis will be recorded.",[13],"Procedure: Total Pulpotomy",{"label":15,"type":10,"description":16,"interventionNames":17},"Radicular Pulpotomy","Inflamed coronal pulp tissue will be removed using a large sterile round bur on a high-speed handpiece with air-water spray, down to the level of the canal orifices. The canal orifices will be located, and the depth of the pulp chamber will be measured using a Williams probe.\n\nA sterile long-shank round carbide bur will be marked with an endodontic file stopper (pulp chamber depth + 3 mm), and radicular pulp tissue will be removed from the canal orifice level to approximately 2-3 mm apical depth.\n\nSmall cotton pellets moistened with 2.5% NaOCl will be individually placed into each canal orifice, down to the level of pulp excision; if necessary, the procedure will be repeated for up to 10 minutes. The time required to achieve hemostasis will be recorded.",[18],"Procedure: Radicular pulpotomy",{"label":20,"type":21,"description":22,"interventionNames":23},"Root Canal Treatment Procedure","ACTIVE_COMPARATOR","After the access cavity is prepared, the vitality of the pulp will be visually confirmed.\n\nOnce the canal orifices are located, the working length (WL) will be determined using a No. 10 K-file and an apex locator, and then confirmed radiographically.\n\nChemomechanical preparation will be performed to the working length using Reciproc files.\n\nAfter every three pecking motions, the root canals will be irrigated with 2.5% NaOCl.\n\nThe final irrigation sequence will be as follows:\n\n* 5 mL of 17% EDTA for 1 minute\n* 5 mL of distilled water\n* 5 mL of 2.5% NaOCl maintained in the canal for 1 minute\n* 5 mL of distilled water (to neutralize NaOCl) After irrigation, canals will be dried with sterile paper points and obturated in a single visit using a calcium silicate-based sealer.",[24],"Procedure: Root canal treatment",[26,31,35],{"type":27,"name":9,"description":28,"armGroupLabels":29,"otherNames":30},"PROCEDURE","Total pulpotomy procedures explained in arm descriptions.",[9],null,{"type":27,"name":32,"description":33,"armGroupLabels":34,"otherNames":30},"Radicular pulpotomy","Radicular pulpotomy procedures explained in arm descriptions.",[15],{"type":27,"name":36,"description":37,"armGroupLabels":38,"otherNames":30},"Root canal treatment","Root canal treatment procedures explained in arm descriptions.",[20],[40,45],{"name":41,"role":42,"phone":43,"phoneExt":30,"email":44},"Efkan Aksay","CONTACT","+905062654889","efkanaksay@gmail.com",{"name":46,"role":42,"phone":47,"phoneExt":30,"email":48},"Merve Sarı, DDS","+905546430401","sarimerve94@outlook.com",[50],{"facility":51,"status":52,"city":53,"state":54,"zip":55,"country":56,"countryCode":30,"cosmosGeoPoint":57,"geoPoint":62,"contacts":63},"Department of Endodontics, Faculty of Dentistry, Hatay Mustafa Kemal University","RECRUITING","Hatay","Antakya","31000","Turkey (Türkiye)",{"type":58,"coordinates":59},"Point",[60,61],27.10486,38.40227,{"lat":61,"lon":60},[64,65],{"name":41,"role":42,"phone":43,"phoneExt":30,"email":44},{"name":46,"role":42,"phone":47,"phoneExt":30,"email":48},{"type":67,"investigatorFullName":68,"investigatorTitle":69,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"PRINCIPAL_INVESTIGATOR","Merve Sari","Assistant Professor","100621819","outcomes-of-pulpotomy-and-root-canal-treatment-in-teeth-with-symptomatic-irreversible-pulpitis-100621819",false,"NCT07375576","Outcomes of Pulpotomy and Root Canal Treatment in Teeth With Symptomatic Irreversible Pulpitis","Evaluation of the Outcomes of Total Pulpotomy, Radicular Pulpotomy, and Root Canal Treatment in Teeth With Extremely Deep Caries and Symptomatic Irreversible Pulpitis","Inclusion Criteria:\n\n* Healthy patients of both sexes, aged between 15 and 45 years, with no systemic diseases, will be screened for inclusion in the study. Strict eligibility criteria will be applied.\n\nThe patients included in the study must have restorable, extremely deep carious lesions in the mandibular first and second molars, and first and second premolars; healthy periodontal status (periodontal pocket ≤ 3 mm); and a clinical diagnosis of symptomatic irreversible pulpitis (history of spontaneous pain, pain persisting after removal of the stimulus, exaggerated and prolonged response to cold testing, and a positive response to the electric pulp test).\n\nExclusion Criteria:\n\n* Teeth with cracks or cusp fractures, subgingival caries, or periapical radiolucency will not be included in the study.\n\nInformed consent will be obtained from all included patients.",true,"ALL","18 Years","45 Years",{"count":82,"type":83},99,"ESTIMATED","INTERVENTIONAL",[86],"NA","The aim of this study is to evaluate the clinical effectiveness of total pulpotomy (TP), radicular pulpotomy (RP), and root canal treatment (RCT) in mandibular premolar and\u002For molar teeth diagnosed with symptomatic irreversible pulpitis, with respect to postoperative pain control and treatment success.Materials and Methods:A total of 99 mandibular premolar and molar teeth will be included in this study. The teeth will be randomly allocated into three groups (n = 33 per group): total pulpotomy, radicular pulpotomy, and root canal treatment.Root canal treatment will be performed using standardized endodontic protocols.Total pulpotomy will be carried out to the level of the canal orifices, followed by hemostasis achieved with 2.5% sodium hypochlorite (NaOCl). A 3-mm-thick layer of mineral trioxide aggregate (MTA) will be placed as the pulpotomy material.Radicular pulpotomy will be performed by removing the pulp tissue a few millimeters apical to the canal orifices. Hemostasis will be achieved using 2.5% NaOCl, and a 3-mm-thick layer of MTA will be placed as the pulpotomy agent.All treated teeth will be restored with glass ionomer cement, followed by a composite resin restoration.Postoperative pain intensity will be assessed using a visual analog scale (VAS) at the following time points: preoperatively, and at 12 hours, 24 hours, 48 hours, and 7 days postoperatively. Clinical and radiographic evaluations will be performed at 3, 6, and 12 months to assess treatment success and periapical health.",[89,90,91],"Post-operative Pain","Pulpitis - Irreversible","Success Rate",[93,94,95,96,97,98,99,100,101],"irreversibl pulpitis","total pulpotomy","radicular pulpotomy","vital pulp therapy (VPT)","root canal treatment (RCT)","pain assessment","vas scale","clinical follow - up","radiographic evaluation","2026-06-04",{"date":104,"type":105},"2026-06-05","ACTUAL",{"date":107,"type":105},"2025-12-01",{"date":109,"type":83},"2027-08-01",{"name":5,"class":6},1]