Ignite Creation Date:
2024-05-06 @ 6:51 PM
Last Modification Date:
2024-10-26 @ 2:55 PM
Study NCT ID:
NCT05801354
Status:
COMPLETED
Last Update Posted:
2023-04-06
First Post:
2023-02-28
Brief Title:
Turmeric Gel as Alternative Non-vital Pulpotomy Medicament in Primary Teeth
Sponsor:
University of Health Sciences Lahore
Organization:
University of Health Sciences Lahore
Study Overview
Official Title:
Turmeric Gel as Alternative Non-Vital Pulpotomy Medicament in Primary Teeth-A Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2023-03
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 purpose of this randomized controlled clinical trial is to use Turmeric gel as non-vital Pulpotomy medicament compared to Formocresol in primary teeth by evaluating its antibacterial effect against Streptococcus mutans and Lactobacillus acidophilus It is hypothesized that there is no difference in the antibacterial effect of Turmeric gel compared with Formocresol when used as non-vital Pulpotomy medicaments
Detailed Description:
It is a multi-arm parallel Randomized Controlled Trial in which forty patients aged between 4 to 8 years each containing at-least one non-vital primary molar will be selected and randomly divided into Group A Formocresol and Group B Turmeric gel Non-vital Pulpotomy will be performed by removing the coronal necrotic pulp Sterile paper point will be dipped in the root canals and taken to the laboratory Cotton pellets soaked in the respective medicaments will be placed over the root canal orifices and filled temporarily Patients will be recalled after one week Samples will be again taken and tooth restored Comparison between bacterial count at baseline and after one week of treatment will be made and expressed as Colony-Forming Unitsml CFUml
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