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Cell-free Autologous Regenerative Endodontics Treatment for Teeth With Periapical Lesions (CARETT) (CARETT)

Primary Purpose

Periapical Diseases, Pulp Necroses

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Autologous Regenerative Endodontic Treatment
Conventional Root Canal Treatment
Sponsored by
Universidad de Valparaiso
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Periapical Diseases focused on measuring Regenerative Endodontics, Permanent Dentition, Pulp Necroses, Periapical Diseases, Root Canal Filling Material

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or female (18-60y) systemically healthy or chronic disease controlled
  • Uniradicular or multiradicular permanent mature teeth
  • Teeth with diagnosis of pulp necrosis (negative response to thermal-cold pulp test) and sings or symptoms (clinical-radiographic) of periapical lesion.
  • Root anatomy with curvatures ≤ 30°
  • Feasibility of adhesive tooth restoration (direct or indirect)
  • Voluntary participation under informed consent

Exclusion Criteria:

  • Pregnant or lactating woman
  • Signs of moderate or severe periodontal disease
  • Teeth with signs of radicular fracture (vertical or horizontal), signs of root resorption (endo-exo)
  • teeth with impossibility of good prognosis of coronary rehabilitation by direct or indirect adhesive technique
  • Teeth that to treat can not to be correctly isolate with rubber dam

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Regenerative Endodontic Treatment

    Conventional root canal treatment

    Arm Description

    This treatment consists of obturated the root canal preparations under an biological-based protocol using autologous biological elements and bioactive materials that allows restore the connective pulp-like tissue within the canals.

    This treatment consist on obturated the root canal preparations under the conventional protocol with an inert biomaterials like guttapercha and endodontics cements to seal the root canals.

    Outcomes

    Primary Outcome Measures

    Efficacy of therapy
    Number of treated tooth that remain in mouth free of clinical (negative percussion, negative palpation, abscence of inflammation, pain and fistula) and radiographic (total or partial reduction on size of periapical lesion) signs or symptoms at 12 month post operatory.

    Secondary Outcome Measures

    Tooth re-sensibilization
    Number of treated tooth that response positively to thermal pulp sensibility test (cold stimulus) after 3, 6 and 12 months post operatory in relation with the initial negative pulp test. The positive-negative pulp sensibility response of treated teeth first is standardized testing the homologous vital tooth on the mouth.
    Tooth re-vitalization
    Number of treated tooth that response positively to Vitality Pulp Test Doppler laser flowmetry after 3, 6 and 12 month. This Vitality Test assess pulpal blood flow by the detection of light scatter generated by moving erythrocytes. The positive-negative pulp vitality response of the treated teeth first is standardized testing the homologous vital tooth on the mouth.
    Periapical lesion resolution
    Resolution of an periapical lesion using Periapical Index (PI), a scoring system for registration of apical periodontitis in radiographs
    Procedure Time
    total time required to perform each of the therapies recorded in minutes

    Full Information

    First Posted
    March 22, 2022
    Last Updated
    March 22, 2022
    Sponsor
    Universidad de Valparaiso
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05305417
    Brief Title
    Cell-free Autologous Regenerative Endodontics Treatment for Teeth With Periapical Lesions (CARETT)
    Acronym
    CARETT
    Official Title
    Cell-free Autologous Regenerative Endodontics Treatment for Permanent Mature Teeth With Pulp Necrosis and Periapical Lesions: a Randomized, Controlled Phase III Clinical Trial (CARETT)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    March 2023 (Anticipated)
    Primary Completion Date
    March 2024 (Anticipated)
    Study Completion Date
    March 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Universidad de Valparaiso

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Conventional endodontic treatment has been the treatment of choice for the management of signs and symptoms of mature permanent teeth with pulpal necrosis and periapical lesion with predictable and favorable results. However, treatment outcomes have not shown improvement or innovation in decades. The main objective of this study is to evaluate the clinical effectiveness of a regenerative endodontic procedure (cell-free and autologous protocol) versus conventional endodontics in the resolution of signs and symptoms of periapical lesion and pulp vitality-sensitivity in mature permanent teeth with a diagnosis of pulpal necrosis and periapical lesion.
    Detailed Description
    Conventional endodontic treatment has been an effective treatment option for decades to treat signs and symptoms in mature permanent teeth with a diagnosis of apical lesion due to pulpal necrosis, allowing the teeth to be kept in the mouth free of signs/symptoms but devitalized. The clinical effectiveness of conventional treatment in this type of case is ≥80%, with some variations according to different studies. Despite advances and modifications in treatment protocols, this therapy has not shown improvements or innovations in its results in recent decades. The Regenerative Endodontics alternative is postulated as a biologically based endodontic treatment option that allows to resolve the signs and symptoms along with dental revitalization through the regeneration of the pulpal connective tissue, generating a substantive possibility of innovation and improvements to the therapy of conventional endodontics. Various regenerative endodontic protocols have been proposed to achieve pulp tissue regeneration, from sophisticated techniques that involve cell transplantation, provision of scaffolds and/or signaling molecules, or simpler protocols that appeal to the autologous capacity of the organism to regenerate tissue. lost. The main objective of this study is to evaluate the clinical effectiveness of a cell-free regenerative endodontic procedure with the contribution of an autologous scaffold (L-PRF) versus conventional endodontics in the recovery of signs of periapical lesion and pulp vitality-sensitivity in mature permanent teeth with diagnosis of pulpal necrosis and periapical lesion.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Periapical Diseases, Pulp Necroses
    Keywords
    Regenerative Endodontics, Permanent Dentition, Pulp Necroses, Periapical Diseases, Root Canal Filling Material

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigatorOutcomes Assessor
    Masking Description
    Participants don´t know wich intervention receive Investigator (outcome evaluator) don´t know wich intervention evaluate Outcomes Assessor (statistics) don´t know wich arm data evaluate
    Allocation
    Randomized
    Enrollment
    228 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Regenerative Endodontic Treatment
    Arm Type
    Experimental
    Arm Description
    This treatment consists of obturated the root canal preparations under an biological-based protocol using autologous biological elements and bioactive materials that allows restore the connective pulp-like tissue within the canals.
    Arm Title
    Conventional root canal treatment
    Arm Type
    Active Comparator
    Arm Description
    This treatment consist on obturated the root canal preparations under the conventional protocol with an inert biomaterials like guttapercha and endodontics cements to seal the root canals.
    Intervention Type
    Procedure
    Intervention Name(s)
    Autologous Regenerative Endodontic Treatment
    Other Intervention Name(s)
    Pulp revascularization, Pulp revitalization, Pulp regeneration
    Intervention Description
    The intervention consist in achieve an access to the teeth root canal system, do a chemico-mechanical preparation each root canal for to be obturated with an autologous biological scaffold and bioactive biomaterials to maintain teeth free of signs/symptoms caused by pulp necroses and periapical lesions
    Intervention Type
    Procedure
    Intervention Name(s)
    Conventional Root Canal Treatment
    Other Intervention Name(s)
    Endodontically-treated Teeth
    Intervention Description
    The intervention consist in achieve an access to the teeth root canal system, do a chemico-mechanical preparation each root canal for to be obturated with an inert biomaterial to maintain teeth free of signs/symptoms caused by pulp necroses and periapical lesions
    Primary Outcome Measure Information:
    Title
    Efficacy of therapy
    Description
    Number of treated tooth that remain in mouth free of clinical (negative percussion, negative palpation, abscence of inflammation, pain and fistula) and radiographic (total or partial reduction on size of periapical lesion) signs or symptoms at 12 month post operatory.
    Time Frame
    12 month
    Secondary Outcome Measure Information:
    Title
    Tooth re-sensibilization
    Description
    Number of treated tooth that response positively to thermal pulp sensibility test (cold stimulus) after 3, 6 and 12 months post operatory in relation with the initial negative pulp test. The positive-negative pulp sensibility response of treated teeth first is standardized testing the homologous vital tooth on the mouth.
    Time Frame
    3, 6 and 12 month
    Title
    Tooth re-vitalization
    Description
    Number of treated tooth that response positively to Vitality Pulp Test Doppler laser flowmetry after 3, 6 and 12 month. This Vitality Test assess pulpal blood flow by the detection of light scatter generated by moving erythrocytes. The positive-negative pulp vitality response of the treated teeth first is standardized testing the homologous vital tooth on the mouth.
    Time Frame
    3, 6 and 12 month
    Title
    Periapical lesion resolution
    Description
    Resolution of an periapical lesion using Periapical Index (PI), a scoring system for registration of apical periodontitis in radiographs
    Time Frame
    3, 6 and 12 month
    Title
    Procedure Time
    Description
    total time required to perform each of the therapies recorded in minutes
    Time Frame
    intraoperatory

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Male or female (18-60y) systemically healthy or chronic disease controlled Uniradicular or multiradicular permanent mature teeth Teeth with diagnosis of pulp necrosis (negative response to thermal-cold pulp test) and sings or symptoms (clinical-radiographic) of periapical lesion. Root anatomy with curvatures ≤ 30° Feasibility of adhesive tooth restoration (direct or indirect) Voluntary participation under informed consent Exclusion Criteria: Pregnant or lactating woman Signs of moderate or severe periodontal disease Teeth with signs of radicular fracture (vertical or horizontal), signs of root resorption (endo-exo) teeth with impossibility of good prognosis of coronary rehabilitation by direct or indirect adhesive technique Teeth that to treat can not to be correctly isolate with rubber dam
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Juan Caro, DDS
    Phone
    +56975242484
    Email
    juancarlos.caro@uv.cl
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Alicia Caro, MSC, DDS
    Organizational Affiliation
    Department of Endodontics, Faculty of Dentistry, University of Valparaíso, Chile.
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Juan Caro, DDS
    Organizational Affiliation
    Department of Endodontics, Faculty of Dentistry, University of Valparaíso, Chile.
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    IPD Sharing Plan Description
    all IPD that underlie results in a publication
    IPD Sharing Time Frame
    from start of participants recruitment to 12 months after publication of results
    IPD Sharing Access Criteria
    The IPD data will be shared with any colleague or researcher that solicited the information by email to principal investigator explaining clear and direct the academic or research intention use of the data
    Citations:
    PubMed Identifier
    33811981
    Citation
    Glynis A, Foschi F, Kefalou I, Koletsi D, Tzanetakis GN. Regenerative Endodontic Procedures for the Treatment of Necrotic Mature Teeth with Apical Periodontitis: A Systematic Review and Meta-analysis of Randomized Controlled Trials. J Endod. 2021 Jun;47(6):873-882. doi: 10.1016/j.joen.2021.03.015. Epub 2021 Mar 31.
    Results Reference
    background
    PubMed Identifier
    16554199
    Citation
    Marquis VL, Dao T, Farzaneh M, Abitbol S, Friedman S. Treatment outcome in endodontics: the Toronto Study. Phase III: initial treatment. J Endod. 2006 Apr;32(4):299-306. doi: 10.1016/j.joen.2005.10.050.
    Results Reference
    background
    PubMed Identifier
    14686806
    Citation
    Friedman S, Abitbol S, Lawrence HP. Treatment outcome in endodontics: the Toronto Study. Phase 1: initial treatment. J Endod. 2003 Dec;29(12):787-93. doi: 10.1097/00004770-200312000-00001.
    Results Reference
    background
    PubMed Identifier
    15107640
    Citation
    Farzaneh M, Abitbol S, Lawrence HP, Friedman S; Toronto Study. Treatment outcome in endodontics-the Toronto Study. Phase II: initial treatment. J Endod. 2004 May;30(5):302-9. doi: 10.1097/00004770-200405000-00002.
    Results Reference
    background
    PubMed Identifier
    23130063
    Citation
    Moazami F, Sahebi S, Sobhnamayan F, Alipour A. Success rate of nonsurgical endodontic treatment of nonvital teeth with variable periradicular lesions. Iran Endod J. 2011 Summer;6(3):119-24. Epub 2011 Aug 15.
    Results Reference
    background
    PubMed Identifier
    22892729
    Citation
    Paredes-Vieyra J, Enriquez FJ. Success rate of single- versus two-visit root canal treatment of teeth with apical periodontitis: a randomized controlled trial. J Endod. 2012 Sep;38(9):1164-9. doi: 10.1016/j.joen.2012.05.021. Epub 2012 Jul 26.
    Results Reference
    background
    PubMed Identifier
    17931388
    Citation
    Ng YL, Mann V, Rahbaran S, Lewsey J, Gulabivala K. Outcome of primary root canal treatment: systematic review of the literature -- Part 2. Influence of clinical factors. Int Endod J. 2008 Jan;41(1):6-31. doi: 10.1111/j.1365-2591.2007.01323.x. Epub 2007 Oct 10.
    Results Reference
    background
    PubMed Identifier
    17931389
    Citation
    Ng YL, Mann V, Rahbaran S, Lewsey J, Gulabivala K. Outcome of primary root canal treatment: systematic review of the literature - part 1. Effects of study characteristics on probability of success. Int Endod J. 2007 Dec;40(12):921-39. doi: 10.1111/j.1365-2591.2007.01322.x. Epub 2007 Oct 10.
    Results Reference
    background
    PubMed Identifier
    27912813
    Citation
    Diogenes A, Ruparel NB. Regenerative Endodontic Procedures: Clinical Outcomes. Dent Clin North Am. 2017 Jan;61(1):111-125. doi: 10.1016/j.cden.2016.08.004.
    Results Reference
    background
    PubMed Identifier
    28211068
    Citation
    Widbiller M, Eidt A, Lindner SR, Hiller KA, Schweikl H, Buchalla W, Galler KM. Dentine matrix proteins: isolation and effects on human pulp cells. Int Endod J. 2018 May;51 Suppl 4:e278-e290. doi: 10.1111/iej.12754. Epub 2017 Mar 14.
    Results Reference
    background
    PubMed Identifier
    25595468
    Citation
    Galler KM, Buchalla W, Hiller KA, Federlin M, Eidt A, Schiefersteiner M, Schmalz G. Influence of root canal disinfectants on growth factor release from dentin. J Endod. 2015 Mar;41(3):363-8. doi: 10.1016/j.joen.2014.11.021. Epub 2015 Jan 13.
    Results Reference
    background
    PubMed Identifier
    22000458
    Citation
    Galler KM, D'Souza RN, Federlin M, Cavender AC, Hartgerink JD, Hecker S, Schmalz G. Dentin conditioning codetermines cell fate in regenerative endodontics. J Endod. 2011 Nov;37(11):1536-41. doi: 10.1016/j.joen.2011.08.027.
    Results Reference
    background
    PubMed Identifier
    21855856
    Citation
    Smith AJ, Scheven BA, Takahashi Y, Ferracane JL, Shelton RM, Cooper PR. Dentine as a bioactive extracellular matrix. Arch Oral Biol. 2012 Feb;57(2):109-21. doi: 10.1016/j.archoralbio.2011.07.008.
    Results Reference
    background
    PubMed Identifier
    26715631
    Citation
    Galler KM. Clinical procedures for revitalization: current knowledge and considerations. Int Endod J. 2016 Oct;49(10):926-36. doi: 10.1111/iej.12606. Epub 2016 Feb 1.
    Results Reference
    background
    PubMed Identifier
    28372291
    Citation
    Ducret M, Fabre H, Celle A, Mallein-Gerin F, Perrier-Groult E, Alliot-Licht B, Farges JC. Current challenges in human tooth revitalization. Biomed Mater Eng. 2017;28(s1):S159-S168. doi: 10.3233/BME-171637.
    Results Reference
    background
    PubMed Identifier
    26195498
    Citation
    Chrepa V, Henry MA, Daniel BJ, Diogenes A. Delivery of Apical Mesenchymal Stem Cells into Root Canals of Mature Teeth. J Dent Res. 2015 Dec;94(12):1653-9. doi: 10.1177/0022034515596527. Epub 2015 Jul 20.
    Results Reference
    background
    PubMed Identifier
    31155298
    Citation
    Arslan H, Ahmed HMA, Sahin Y, Doganay Yildiz E, Gundogdu EC, Guven Y, Khalilov R. Regenerative Endodontic Procedures in Necrotic Mature Teeth with Periapical Radiolucencies: A Preliminary Randomized Clinical Study. J Endod. 2019 Jul;45(7):863-872. doi: 10.1016/j.joen.2019.04.005. Epub 2019 May 31.
    Results Reference
    background
    PubMed Identifier
    31708612
    Citation
    Jha P, Virdi MS, Nain S. A Regenerative Approach for Root Canal Treatment of Mature Permanent Teeth: Comparative Evaluation with 18 Months Follow-up. Int J Clin Pediatr Dent. 2019 May-Jun;12(3):182-188. doi: 10.5005/jp-journals-10005-1616.
    Results Reference
    background
    PubMed Identifier
    32202965
    Citation
    Brizuela C, Meza G, Urrejola D, Quezada MA, Concha G, Ramirez V, Angelopoulos I, Cadiz MI, Tapia-Limonchi R, Khoury M. Cell-Based Regenerative Endodontics for Treatment of Periapical Lesions: A Randomized, Controlled Phase I/II Clinical Trial. J Dent Res. 2020 May;99(5):523-529. doi: 10.1177/0022034520913242. Epub 2020 Mar 23.
    Results Reference
    background
    PubMed Identifier
    32950179
    Citation
    About I. Proceedings of the Pulp Biology and Regeneration Group Symposium 2019: Bridging Basic and Translational Research in Pulp Biology-Developing Technologies for Regenerating Vital Dental Tissues. J Endod. 2020 Sep;46(9S):S1. doi: 10.1016/j.joen.2020.06.018. No abstract available.
    Results Reference
    background
    PubMed Identifier
    28844305
    Citation
    He L, Kim SG, Gong Q, Zhong J, Wang S, Zhou X, Ye L, Ling J, Mao JJ. Regenerative Endodontics for Adult Patients. J Endod. 2017 Sep;43(9S):S57-S64. doi: 10.1016/j.joen.2017.06.012.
    Results Reference
    background

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    Cell-free Autologous Regenerative Endodontics Treatment for Teeth With Periapical Lesions (CARETT)

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