Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06524076
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-22
Brief Title:
Evaluation of Success Rate of Partial Pulpotomy Versus Complete Pulpotomy in Primary Molars Using NeoPUTTY MTA
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Clinical and Radiographic Evaluation of Partial Pulpotomy Versus Complete Pulpotomy in Vital Pulp Therapy in Primary Molars Using NeoPUTTY MTA Randomized Clinical Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Evaluating the clinical and radiographic success of partial pulpotomy compared to complete pulpotomy in vital primary second molars with reversible pulpitis using NeoPUTTY MTA
Detailed Description:
Children with symptoms of reversible pulpitis in their second primary molar will be chosen to be enrolled in the study and then randomly allocated into two groups One group will undergo partial pulpotomy and the other group complete pulpotomy and followed up for 12 months The blinding of the operator is not possible due to the nature of the technique used Trial participants outcome assessors and statistician will be blinded
1 Informed consent from participating childrens parents
2 Baseline records photographs percussion test periapical radiograph and personal data collection
3 Diagnostic chart with personal medical and dental history will be filled
4 Allocation concealed by withdrawing a sealed opaque envelope containing Four-folded numbered papers containing the type of vital pulp therapy technique that will be used then writing the patients name and ID on it and will be opened after removing the carious lesion
5 Clinical examination will be performed to assess the clinical inclusion criteria Pulpal and periapical diagnoses are established after clinical examination
6 Preoperative and Postoperative photographs will be taken
1 Informed consent from participating childrens parents
2 Baseline records photographs percussion test periapical radiograph and personal data collection
3 Diagnostic chart with personal medical and dental history will be filled
4 Allocation concealed by withdrawing a sealed opaque envelope containing Four-folded numbered papers containing the type of vital pulp therapy technique that will be used then writing the patients name and ID on it and will be opened after removing the carious lesion
5 Clinical examination will be performed to assess the clinical inclusion criteria Pulpal and periapical diagnoses are established after clinical examination
6 Preoperative and Postoperative photographs will be taken
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None