Ignite Creation Date:
2024-05-06 @ 2:49 PM
Last Modification Date:
2024-10-26 @ 1:37 PM
Study NCT ID:
NCT04430998
Status:
UNKNOWN
Last Update Posted:
2020-06-18
First Post:
2020-06-06
Brief Title:
Efficacy of Zinc L-Carnosine Mouth Rinse
Sponsor:
University of Milan
Organization:
University of Milan
Study Overview
Official Title:
Efficacy of a Zinc-L-Carnosine -Based Mouth Rinse on Periodontal Tissues and Pain After Scaling and Root Planing - a Randomized Clinical Trial a Randomized Controlled Trial
Status:
UNKNOWN
Status Verified Date:
2020-06
Last Known Status:
NOT_YET_RECRUITING
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:
A clinical trial to assess the effect of a Zinc-L-Carnosine-based mouth rinse on periodontal tissues and pain after scaling and root planing
Detailed Description:
A randomized double blind 3 group parallel study with random allocation of 75 patients to any of three groups Zinc-L-Carnosine-based mouth rinse Chlorhexidine mouth rinse and placebo water control Three days after professional oral hygiene which aimed at the normalization of the periodontal index the primary HI VAS and secondary mSBI FMPS VMI SI outcomes of the study are measured to obtain baseline information and then scaling and root planing are carried out
The participants will be advised to follow their regular oral hygiene procedures tooth brushing in addition to the allocated mouth rinse They will be examined again for primary and secondary outcomes at 7 and 21 days
Clinical evaluation
Clinical examination of each participant will be done by a single examiner using the previously described VAS scale and a UNC periodontal probe No 5 explorer Hu-Friedy Chicago Ill In addition to these indices each subject will be asked to report any adverse events they have encountered during the experiment
The participants will be advised to follow their regular oral hygiene procedures tooth brushing in addition to the allocated mouth rinse They will be examined again for primary and secondary outcomes at 7 and 21 days
Clinical evaluation
Clinical examination of each participant will be done by a single examiner using the previously described VAS scale and a UNC periodontal probe No 5 explorer Hu-Friedy Chicago Ill In addition to these indices each subject will be asked to report any adverse events they have encountered during the experiment
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