Pulpotomy Clinical Trial
Official title:
Clinical and Radiographic Evaluation of Vital Pulpotomy Techniques in Primary Molars Using of Premixed Bioactive Bioceramic MTA (Neo-putty) as a Novel Pulpotomy Medication Versus Formocresol: A Randomized Clinical Trial.
Despite the benefit of formocresol, there are toxic effects allergic reactions and local soft and hard tissue necrosis have been reported when such formaldehyde compounds were used clinically, however, the adverse effect of the clinically used of this compound are not widely reported. It has been stated that it has a side effect on the permanent successor although it results as a successful technique for the treatment of the primary teeth
The rationale for conducting the research: Nowadays, the introduction of new Bio-inductive materials resulted in the shift of the concept of preservation of radicular pulp tissue to regeneration. Restoration of the anatomical continuity of damaged tissue and disturbed functional status of the radicular pulp tissue require an appropriate method of wound healing which includes well-organized, biochemical and cellular events, leading to the growth and regeneration of injured radicular tissue in a special manner. A higher standard in bioactive bioceramic putty as manufacture claimed the Neo-Putty® NuSmile is a bioactive bioceramic premixed root and pulp treatment with superior handling properties, promoting hydroxyapatite formation to support the healing process. Neo-Putty® is a premixed bioactive bioceramic root & pulp treatment consisting of an extremely fine, inorganic powder of tricalcium/dicalcium silicate in a water free organic liquid. The product is packaged ready to use. No mixing is required. Neo-Putty® is designed to set in vivo in the presence of moisture from the surrounding tissues. Considering the limitations of these data, we are conduction this clinical trial. The outcomes of this study will have a substantial impact on clinical practice for pediatric patients, as well as patient care, around the world. Aim of the study: This randomized clinical trial study will assess clinically and radiographically, the effect of Neo-Putty® as a pulp medicament following coronal pulp amputation in children's primary molars with carious pulp exposure in comparison to Formocresol (FC). Research question: Is the pulpotomy procedure in primary molars using premixed Bioactive bioceramic MTA (Neo-putty) more clinically successful than Formocresol? PICOS: P: Carious primary molars with no spontaneous or provoked pain (vital primary molars) I: Neo-Putty® as dressing agents in pulpotomized primary molars C: Formocresol Pulpotomy (FC) O: Clinical Success S: In-Vivo Study II. Methods Study Design: Study Type: Interventional (Clinical Trial) Estimated Enrolment: 88 participants Allocation: Randomized Intervention Model: Parallel Assignment Primary Purpose: Treatment Official Title: Clinical and Radiographic Evaluation of Vital Pulpotomy in Primary Molars using of premixed Bioactive bioceramic MTA (Neo-putty) as a Novel Pulpotomy Medication versus Formocresol: A Randomized Clinical Trial. Estimated Study Start Date: December 2023 Estimated Primary Completion Date: January 2024 Trial design: The study is a randomized clinical trial (RCT) where 2 arm parallel groups with a 1:1 allocation ratio were compared. The child participants and the legal guardian of each participating child and the statistician were blinded. Interventions In the control group: a cotton pellet moistened with full-strength FC will be placed for 5 minutes on the amputated pulp, after reaching hemostasis. The pulp stumps will be then covered by IRM. In the Intervention group: Neo-Putty® as dressing agents in pulpotomized primary molars. Following removal of the coronal pulp with a round bur and hemostasis, the pulp stumps in the study group will be covered with Neo-Putty ® according to the manufacturer's instructions. Neo-Putty will be placed in the prepared cavity, and then covered with a reinforced Zinc Oxide-Eugenol (IRM, Bayer-Leverkussen, Germany). Outcome Measures: 1. Primary outcome: Clinical success [Time Frame: 12 months]. - Success clinically and radiographically will assess by the number of participants with symptoms-free and no peri-radicular pathology (at 3,6,9and 12 months) - No clinical or radiographic evidence of pulp degeneration, such as spontaneous pain, excessive bleeding from the root canal, internal root resorption, inter-radicular and/or periapical bone destruction, swelling, or sinus tract. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT01878851 -
Characterization of Blood Drawn From the Pulp of Primary Molar Undergoing Pulpotomy or Pulpectomy.
|
||
Completed |
NCT04270318 -
Sodium Hypoclorite as an Antibacterial Agent Prior to Pulpotomies
|
N/A | |
Completed |
NCT04909827 -
3D-printed Endocrowns Versus Prefabricated Zirconia Crowns in Pulpally-treated Primary Molars
|
Phase 4 | |
Completed |
NCT03200938 -
Clinical Applicability of PBS® CIMMO Cement in Pulpotomies
|
N/A | |
Recruiting |
NCT04863222 -
Clinical and Radiographic Success of MTA vs Biodentine
|
Phase 4 | |
Active, not recruiting |
NCT05554952 -
Indirect Pulp Capping Versus Pulpotomy With MTA for Treatment of Primary Molars With Deep Caries
|
N/A | |
Completed |
NCT03779698 -
BiodentineTM Versus Formocresol Pulpotomy Technique in Primary Molars
|
Phase 4 | |
Completed |
NCT03395496 -
Comparison of Biodentine and MTA Pulpotomies in the Primary Molar Teeth 3 Year Follow up
|
Early Phase 1 | |
Not yet recruiting |
NCT05747300 -
Wellroot PT Versus MTA in Pulpotomy of Primary Molars
|
N/A | |
Not yet recruiting |
NCT06219824 -
Clinical and Radiographic Evaluation of Bioceramic Putty MTA Versus MTA in Pulpotomy of Immature Permanent Molars
|
Phase 3 | |
Completed |
NCT03718676 -
Pulpotomy With Various MTA Materials and Ferric Sulphate
|
N/A | |
Recruiting |
NCT05279820 -
Comparative Study of the Outcome of Partial and Full Pulpotomy in Irreversible Pulpits
|
N/A | |
Active, not recruiting |
NCT02298504 -
Vital Pulp Treatment in Primary Teeth
|
Phase 4 | |
Completed |
NCT04010929 -
Efficacy of Er,Cr:YSGG Laser in Partial Pupotomy
|
N/A | |
Terminated |
NCT02783911 -
Comparison of Mineral Trioxide Aggregate (MTA) & Ferric Sulfate (FS) Pulpotomies
|
N/A | |
Withdrawn |
NCT02393326 -
Biodentine Partial Pulpotomy of Pulpally Exposed Primary Molars
|
N/A | |
Completed |
NCT05792748 -
Comparison of Zinc Oxide Eugenol to Ferric Sulphate Pulpotomy in Primary Teeth
|
N/A | |
Completed |
NCT05680285 -
Evaluation of Low Level Laser Therapy in Primary Tooth Pulpotomy Treatment
|
N/A | |
Completed |
NCT05297344 -
Clinical Study of the Direct Pulp Capping in Primary Teeth
|
N/A | |
Completed |
NCT03782714 -
Low-level Laser Therapy Versus Formocresol in Primary Molar Pulpotomies
|
N/A |