Ignite Creation Date:
2024-07-17 @ 11:14 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06468085
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-06-21
First Post:
2024-06-15
Brief Title:
Evaluation of Pulpotomy Using Two Different Agents in Mature Anterior Teeth With Pulpitis
Sponsor:
Ain Shams University
Organization:
Ain Shams University
Study Overview
Official Title:
Clinical and Radiographic Evaluation of Premixed Bioceramic Putty and Biodentine Pulpotomy in Mature Permanent Anterior Teeth With Signs of Pulpitis A Randomized Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
the study will evaluate the clinical and radiological success of mature permanent anterior teeth pulpotomy in children and adolescents with signs of pulpitis using two different Biomimetic materials NeoPutty and Biodentine as a pulp dressing material in comparison to root canal treatment at 3 6 9 and 12 months follow up
Detailed Description:
In this randomized controlled trial A total number of 75 mature vital permanent anterior teeth with recent trauma or deep caries in children aged between 9 and 14 years will be included Patients will be randomly allocated into three study groups group A premixed bioceramic NeoPutty test group group B Biodentine test group and group C root canal treatment control group Cases will be evaluated clinically and radiographically to obtain baseline data Local anesthesia will be administered and then rubber dam isolation will be performed Pulpotomy procedure will be performed after hemostasis followed by covering pulp stump with Premixed Bioceramic or Biodentine according to the corresponding group then final composite restoration will be applied Root canal treatment will be performed to the control group followed by composite restoration Blinded clinical evaluation will be done at baseline 3 6 9 and 12 months
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None