Ignite Creation Date:
2024-06-16 @ 11:49 AM
Last Modification Date:
2024-10-26 @ 3:30 PM
Study NCT ID:
NCT06435065
Status:
RECRUITING
Last Update Posted:
2024-05-30
First Post:
2024-05-17
Brief Title:
Direct Pulp Capping Agent on Human Pulp Tissue
Sponsor:
DR SURINDER SACHDEVA
Organization:
Maharishi Markendeswar University Deemed to be University
Study Overview
Official Title:
Histological and Radiographic Evaluation of the Effects of Direct Pulp Capping Agent on Human Pulp Tissue
Status:
RECRUITING
Status Verified Date:
2024-05
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:
This in- vivo study was conducted to evaluate the response of human pulp tissue following direct pulp capping using four different pulp capping agents in premolars scheduled for extraction in patients undergoing orthodontic treatment
Detailed Description:
For the study 40 premolars from patients in the age group of 15-25 years undergoing orthodontic treatment in the Department of Orthodontics MMCDSR Mullana Ambala who had to get their premolars extracted as per their orthodontic treatment plan will be selected
Only healthy premolars with no caries showing no signs and symptoms of pulpitis or periodontal diseases were selected Medically compromised patients or teeth with radiographic findings of externalinternal resorption bone loss or calcifications in the pulp chamber will be excluded from the study The selected premolars were then randomly divided into four equal groups namely GROUP I - Direct pulp capping procedure performed using Biodentine GROUP II - Direct pulp capping procedure performed using MTA GROUP III - Direct pulp capping procedure performed using TheraCal LC GROUP IV - Direct pulp capping procedure performed using Tristrontium aluminate
The direct pulp capping procedure was carried out under rubber dam The study protocol included class I cavity preparations on the premolars followed by iatrogenic exposure of the pulp 05mm using a sterile round bur placement of the direct pulp capping agent according to the material of allotted to the study group The teeth were permanently restored on the same visit except for MTA group were the teeth were temporarily restored using Cavit G and recalled after 1 day for permanent restoration The patients were then enquired for any 94 SUMMARY 95 symptoms at 1 day and 7 days post operatively The teeth were then atraumatically extracted 3 months after the procedure The extracted teeth were then put to CBCT as well as histopathological examination Through CBCT evaluation the completeness of the dentine bridge was evaluated Histopathological examination was done to examine the pulpal response and the quality of the dentine bridge formed
Only healthy premolars with no caries showing no signs and symptoms of pulpitis or periodontal diseases were selected Medically compromised patients or teeth with radiographic findings of externalinternal resorption bone loss or calcifications in the pulp chamber will be excluded from the study The selected premolars were then randomly divided into four equal groups namely GROUP I - Direct pulp capping procedure performed using Biodentine GROUP II - Direct pulp capping procedure performed using MTA GROUP III - Direct pulp capping procedure performed using TheraCal LC GROUP IV - Direct pulp capping procedure performed using Tristrontium aluminate
The direct pulp capping procedure was carried out under rubber dam The study protocol included class I cavity preparations on the premolars followed by iatrogenic exposure of the pulp 05mm using a sterile round bur placement of the direct pulp capping agent according to the material of allotted to the study group The teeth were permanently restored on the same visit except for MTA group were the teeth were temporarily restored using Cavit G and recalled after 1 day for permanent restoration The patients were then enquired for any 94 SUMMARY 95 symptoms at 1 day and 7 days post operatively The teeth were then atraumatically extracted 3 months after the procedure The extracted teeth were then put to CBCT as well as histopathological examination Through CBCT evaluation the completeness of the dentine bridge was evaluated Histopathological examination was done to examine the pulpal response and the quality of the dentine bridge formed
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