Ignite Creation Date:
2024-05-06 @ 10:28 AM
Last Modification Date:
2024-10-26 @ 12:30 PM
Study NCT ID:
NCT03262701
Status:
TERMINATED
Last Update Posted:
2022-12-21
First Post:
2017-08-22
Brief Title:
Adjunctive Hydrogen Peroxide for Periodontal Therapy
Sponsor:
Loma Linda University
Organization:
Loma Linda University
Study Overview
Official Title:
Custom Tray Application of Peroxide Gel as an Adjunct to Scaling and Root Planing in the Treatment of Periodontitis A 6-Month Randomized Trial
Status:
TERMINATED
Status Verified Date:
2022-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
COVID
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
AHP
Brief Summary:
There have been many adjunctive treatments for the additional clinical benefits to scaling and root planing SRP in the treatment of chronic periodontitis Topical hydrogen peroxide HP delivered in a custom fabricated tray has been shown to improve pocket depth PD and inflammation The purpose of this study is to assess the adjunctive treatment outcome of HP gel in custom tray application in individuals with chronic periodontitis receiving SRP The purpose of this investigator-initiated study is to evaluate and compare the clinical effects of scaling and root planing SRP combined with local delivery of 17 hydrogen peroxide HP gel in customized trays to that of SRP alone
Detailed Description:
Hydrogen peroxide HP has been used in for wound debridement and oral rinses in dentistry for a few decades It is widely available in a bottle of 3 in liquid The use of hydrogen peroxide in gel type in 17 as an adjunct to conventional periodontal therapy has been introduced but there are limited information on the efficacy The current study is to design to evaluate the adjunctive treatment outcome of hydrogen peroxide gel in custom tray application in individuals with chronic periodontitis receiving non surgical therapy scaling and root planingSRP To test the adjunct effect of HP gel in tray there will be three parallel arms one with the gel for the period of 26 week one with the gel for 13 weeks and control group without the gel
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
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