Ignite Creation Date:
2024-05-06 @ 3:10 PM
Last Modification Date:
2024-10-26 @ 1:44 PM
Study NCT ID:
NCT04547764
Status:
COMPLETED
Last Update Posted:
2020-09-14
First Post:
2020-07-11
Brief Title:
Evaluation of Triple Antibiotic Paste Pulp Therapy Compared to Vitapex in Primary Molars
Sponsor:
King Abdulaziz University
Organization:
King Abdulaziz University
Study Overview
Official Title:
Clinical and Radiographic Evaluation of Triple Antibiotic Paste Pulp Therapy Compared to Vitapex Pulpectomy in Non-vital Primary Molars
Status:
COMPLETED
Status Verified Date:
2020-09
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 the study was to compare the clinical and radiographic success of triple antibiotic paste TAP which includes metronidazole ciprofloxacin and minocycline and Vitapex calcium hydroxideiodoform paste for root canal treatment of pulpally involved teeth
Detailed Description:
This study evaluated and compared the clinical and radiographic efficacy of non-instrumentation triple antibiotic paste pulp therapy TAP versus Vitapex pulpectomy in non-vital primary molars Healthy 5 to 9 years old children with at least one non-vital primary molar were included in the study molars were divided based on the subjects cooperation level and parental preference into two groups In the first group molars received TAP and in the second group they received Vitapex pulpectomy followed by a stainless-steel crown The TAP was freshly prepared and proportioned in equal parts by volume metronidazole minocycline and ciprofloxacin111 before the scheduled treatment appointment The clinical and radiographic examination was performed by two calibrated and trained pediatric dentists at the pre-operative baseline and at the six- and 12-months follow-up visits
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?:
False
Is an FDA AA801 Violation?:
None