Ignite Creation Date:
2024-05-06 @ 12:56 PM
Last Modification Date:
2024-10-26 @ 1:06 PM
Study NCT ID:
NCT03890835
Status:
UNKNOWN
Last Update Posted:
2019-03-26
First Post:
2019-03-17
Brief Title:
Pulpotomy in Mature Permanent Molars Using Biodentine Versus MTA
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
Comparative Evaluation of Postoperative Pain and Success Rate After Pulpotomy in Mature Permanent Molars Using Biodentine Versus Mineral Trioxide Aggregate MTA as Capping Materials A Randomized Clinical Trial
Status:
UNKNOWN
Status Verified Date:
2019-03
Last Known Status:
NOT_YET_RECRUITING
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 aim of this study is to compare treatment outcomes of pulpotomy in mature permanent teeth using Biodentine versus MTA regarding postoperative pain and success rate
Detailed Description:
Patients will be clinically and radiographically examined and their eligibility will be assessed
Eligible patients will be randomly assigned to one of 2 groups experimental group pulpotomy using Biodentine and the control group pulpotomy using MTA
After adminsrtation of local anesthesia pulpotomy will be done under rubber dam isolation The pulp tissue will be removed until the level of the orifices of the canals After hemostasis is achieved the capping material will be placed In the experimental group the capping material is Biodentine while in the control group the capping material is MTA
The cavities will be sealed with resin-modified glass ionomer Then the teeth will be permanently restored with composite A post-operative radiograph will be taken
The patients will be given a pain diary based on Numerical Rating Scale NRS and asked to rate their pain level at the specified times
The patients will be recalled after 6 and 12 months post-operatively
Eligible patients will be randomly assigned to one of 2 groups experimental group pulpotomy using Biodentine and the control group pulpotomy using MTA
After adminsrtation of local anesthesia pulpotomy will be done under rubber dam isolation The pulp tissue will be removed until the level of the orifices of the canals After hemostasis is achieved the capping material will be placed In the experimental group the capping material is Biodentine while in the control group the capping material is MTA
The cavities will be sealed with resin-modified glass ionomer Then the teeth will be permanently restored with composite A post-operative radiograph will be taken
The patients will be given a pain diary based on Numerical Rating Scale NRS and asked to rate their pain level at the specified times
The patients will be recalled after 6 and 12 months post-operatively
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