Viewing Study NCT06433245



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06433245
Status: RECRUITING
Last Update Posted: 2024-05-29
First Post: 2024-05-22

Brief Title: Outcome Following Use of Different Concentrations of NaOCl as Wound Lavage and Hemostatic Agent in Partial Pulpotomy
Sponsor: Postgraduate Institute of Dental Sciences Rohtak
Organization: Postgraduate Institute of Dental Sciences Rohtak

Study Overview

Official Title: Outcome Following Use of Different Concentrations of Sodium Hypochlorite as Wound Lavage and Hemostatic Agent in Partial Pulpotomy A Randomised Control Trial
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: The aim of this randomised control trial is to compare the effect of different concentrations of NaOCl on outcome of partial pulpotomy in teeth with clinical signs indicative of irreversible pulpitis

The main question it aims to answer are

1 clinical and radiographic outcome of partial pulpotomy following use of 5 and 3 NaOCl in mature permanent teeth with clinical signs indicative of irreversible pulpitis
2 OHRQoL and pain experience after use of 5 and 3 NaOCl during partial pulpotomy in teeth with clinical signs indicative of irreversible pulpitis
Detailed Description: TITLE - Outcome following use of different concentrations of NaOCl as wound lavage and hemostatic agent in partial pulpotomy A Randomised control trial

Question it aims to answer

Does pulpal lavage using 3 and 5 sodium hypochlorite have comparable effect on outcome of partial pulpotomy in mature permanent teeth with clinical signs of irreversible pulpitis P Population -Mature permanent mandibular molars with signs of irreversible pulpitis

I Intervention - 5 NaOCl C Comparison - 3 NaOCl O Outcome - 1 Assessment of clinical and radiographic success at 12 months of follow up

2 Assessment of OHRQoL and pain experience at baseline post-operatively every 24 hours for 1 week and OHRQoL at 6 and 12 months

In literature pertaining to vital pulp therapy procedures there is often a focus on comparing various materials or treatment methodologies However the use of sodium hypochlorite holds significant importance in ensuring the successful outcome of the procedure The previous studies indicate that the use of NaOCl presents as a confounding factor compounded by variations among operators in their choice of high and low concentrations of NaOClSo there is a pressing need for a direct comparative analysis to assess the influence of varying sodium hypochlorite concentrations on the overall efficacy and success rates of vital pulp therapy procedures

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