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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03813433
Other study ID # pedodontic department cairo
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 2023
Est. completion date November 2024

Study information

Verified date September 2021
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the objective of this study is to evaluate post operative pain after using Endosequence versus Mineral Trioxide Aggregate as coronal plug material in revascularization of non vital immature anterior teeth


Description:

The treatment of immature young permanent anterior teeth is challenging because in addition of the need of elimination of bacterial infection; the lack of natural apical constriction against which a suitable filling material can be placed is considered the main problem. In the past many different treatments have been proposed for immature permanent teeth with necrotic pulps such as:Custom fitting of filling materials like gutta percha, Periapical surgeries, apexification. The disadvantages of these treatments are: the compromised Crown/root ratio, possibility of vertical fracture. Pulp revascularization is dependent on the ability of residual pulp and apical and periodontal stem cells to differentiate. These cells have the ability to generate a highly vascularized and rich living tissue. MTA was chosen as coronal seal to be placed over the blood clot due its a biocompatibility, bio-inductivity. However, the disadvantages of MTA are: discoloration of the coronal dentine when placed in the canal and the difficult handling properties. Recently, a new bioceramic material has been introduced to the market, namely, EndoSequence which is bioactive, has antibacterial activity, less cytotoxic effect and similar antimicrobial properties, maintain color stability of the tooth when compared to MTA


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 24
Est. completion date November 2024
Est. primary completion date November 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 14 Years
Eligibility Inclusion Criteria: - Age of patient range from 8-14 y. - Patients are free from any systemic diseases that may hinder the normal healing process. - Non vital permanent anterior teeth with open apex. - Pulp space not needed for post and core for final restoration. - Compliant patient/parent. Exclusion Criteria: - Patients having allergy to medicaments and antibiotics necessary to complete the procedure. - Tooth with vital pulp or complete root formation. - Teeth with internal or external root resorption. - Un-cooperative patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Revascularization
a procedure used to regenerate pulp dentin complex that restores the functional properties of this immature anterior teeth, prevent and resolves apical periodontitis

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary discoloration Asking patient question (Binary:present or absent) 1 month
Primary discoloration Asking patient question (Binary:present or absent) 3 months
Primary dicoloration Asking patient question (Binary:present or absent) 6 months
Primary discoloration Asking patient question (Binary:present or absent) 9 months
Primary discoloration Asking patient question (Binary:present or absent) 12months
Secondary post operative pain asking the patient (Binary: present or Absent) 1,3, 6, 9 and 12 months
Secondary color stability Operator and supervisor evaluation (Using shade guide) 1,3, 6, 9 and 12 months
Secondary Pain on percussion Assessed by back of the mirror (Binary: present or absent) 1,3, 6, 9 and 12 months
Secondary Swelling assessed by visual examination (Binary:present or absent) 1,3, 6, 9 and 12 months
Secondary Sinus or fistula assessed by visual examination (Binary:present or absent) 1,3, 6, 9 and 12 months
Secondary Root lengthening assessed radiographically (DIGORA® for Windows software) 6 and 12 months
See also
  Status Clinical Trial Phase
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Active, not recruiting NCT03763110 - Photo-Activated Disinfection Versus Triple-Antibiotic Paste for Management of Necrotic Young Permanent Anterior Teeth N/A
Completed NCT00881907 - Tissue Characterization in Teeth Treated With a Regeneration Protocol Phase 0
Recruiting NCT04313010 - Effectiveness of Regenerative Endodontics Therapy for Single-rooted Mature Permanent Tooth With Pulp Necrosis N/A
Completed NCT03589560 - Evaluation of Biodentine and Mineral Trioxide Aggregate in Revascularization of Non Vital Immature Anterior Teeth N/A
Not yet recruiting NCT03717337 - Success Rate of Single Versus Two Visit Regenerative Treatment Protocol in Non Vital Mature Anterior Teeth N/A
Completed NCT01817413 - Comparison of Two Dental Techniques Used to Treat Teeth Which Have Become Infected or Painful Following Trauma Phase 4
Completed NCT03849222 - Evaluation the Effect of Using of Apical Matrix With Apexification Procedure on Apical Healing of Necrotic Immature Teeth Phase 2/Phase 3
Completed NCT00881491 - Treatment Outcome With a Revascularization Protocol Using the Triple Versus Double Antibiotic Paste Phase 0